Trial Outcomes & Findings for Brain Safe: Consumer Intervention to Reduce Exposure to Drugs Linked to Alzheimer's Disease (NCT NCT04121858)
NCT ID: NCT04121858
Last Updated: 2026-07-20
Results Overview
To calculate the Total Standardized Daily Dose (TSDD), we first calculated the Standardized Daily Dose (SDD) for each anticholinergic medication with an ACB Score of 2 or 3. SDD was calculated by multiplying the strength by the units per dose and frequency per day and number of refills. The product was divided by the minimum effective daily dose (where available) or the minimum effective geriatric dose to standardize the quantity across multiple classes of medications. The SDD for all anticholinergics with an ACB score 2 or 3 was then summed for each participant for each 6-month period, and divided by the number of days in the relevant six month period to arrive at a TSDD. Range: The minimum possible value is 0 (optimal outcome; indicating zero exposure to ACB 2 or 3 medications). There is no fixed theoretical maximum score(higher value more exposure), as the upper limit is mathematically determined by the total volume and combination of medications a participant is prescribed.
COMPLETED
NA
706 participants
Baseline, 6 months, 12 Months
2026-07-20
Participant Flow
21 participants consented but were not randomized.
Participant milestones
| Measure |
Brain Safe App
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
Attention Control App
1\) Attention Control App provides a medication list for older patients to use but lacks the conversation starters for patient to use with there physicians aimed at reduction in exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
|---|---|---|
|
Overall Study
STARTED
|
342
|
343
|
|
Overall Study
6 Month
|
278
|
269
|
|
Overall Study
12 month
|
251
|
240
|
|
Overall Study
Primary Outcome
|
297
|
293
|
|
Overall Study
COMPLETED
|
251
|
240
|
|
Overall Study
NOT COMPLETED
|
91
|
103
|
Reasons for withdrawal
| Measure |
Brain Safe App
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
Attention Control App
1\) Attention Control App provides a medication list for older patients to use but lacks the conversation starters for patient to use with there physicians aimed at reduction in exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
|---|---|---|
|
Overall Study
Lost to Follow-up
|
46
|
53
|
|
Overall Study
Withdrawal by Subject
|
40
|
41
|
|
Overall Study
Death
|
3
|
7
|
|
Overall Study
No longer eligible
|
2
|
2
|
Baseline Characteristics
Missing data
Baseline characteristics by cohort
| Measure |
Brain Safe App
n=342 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
Attention Control App
n=343 Participants
1\) Attention Control App provides a medication list for older patients to use but lacks the conversation starters for patient to use with there physicians aimed at reduction in exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Total
n=685 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Continuous
|
69.63 Years
STANDARD_DEVIATION 6.73 • n=340 Participants • Missing data
|
69.06 Years
STANDARD_DEVIATION 6.19 • n=340 Participants • Missing data
|
69.35 Years
STANDARD_DEVIATION 6.47 • n=680 Participants • Missing data
|
|
Sex: Female, Male
Female
|
262 Participants
n=340 Participants • Missing data
|
259 Participants
n=340 Participants • Missing data
|
521 Participants
n=680 Participants • Missing data
|
|
Sex: Female, Male
Male
|
78 Participants
n=340 Participants • Missing data
|
81 Participants
n=340 Participants • Missing data
|
159 Participants
n=680 Participants • Missing data
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
5 Participants
n=342 Participants
|
7 Participants
n=343 Participants
|
12 Participants
n=685 Participants
|
|
Race (NIH/OMB)
Asian
|
2 Participants
n=342 Participants
|
1 Participants
n=343 Participants
|
3 Participants
n=685 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=342 Participants
|
1 Participants
n=343 Participants
|
1 Participants
n=685 Participants
|
|
Race (NIH/OMB)
Black or African American
|
37 Participants
n=342 Participants
|
36 Participants
n=343 Participants
|
73 Participants
n=685 Participants
|
|
Race (NIH/OMB)
White
|
288 Participants
n=342 Participants
|
290 Participants
n=343 Participants
|
578 Participants
n=685 Participants
|
|
Race (NIH/OMB)
More than one race
|
7 Participants
n=342 Participants
|
5 Participants
n=343 Participants
|
12 Participants
n=685 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
3 Participants
n=342 Participants
|
3 Participants
n=343 Participants
|
6 Participants
n=685 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
10 Participants
n=342 Participants
|
4 Participants
n=343 Participants
|
14 Participants
n=685 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
330 Participants
n=342 Participants
|
336 Participants
n=343 Participants
|
666 Participants
n=685 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
2 Participants
n=342 Participants
|
3 Participants
n=343 Participants
|
5 Participants
n=685 Participants
|
|
Highest Level of Education
Grade/Middle/Some High School
|
10 Participants
n=342 Participants
|
8 Participants
n=343 Participants
|
18 Participants
n=685 Participants
|
|
Highest Level of Education
High School Graduate or GED
|
48 Participants
n=342 Participants
|
67 Participants
n=343 Participants
|
115 Participants
n=685 Participants
|
|
Highest Level of Education
Some College
|
76 Participants
n=342 Participants
|
82 Participants
n=343 Participants
|
158 Participants
n=685 Participants
|
|
Highest Level of Education
College Degree
|
118 Participants
n=342 Participants
|
97 Participants
n=343 Participants
|
215 Participants
n=685 Participants
|
|
Highest Level of Education
Masters or other advanced degree
|
81 Participants
n=342 Participants
|
73 Participants
n=343 Participants
|
154 Participants
n=685 Participants
|
|
Highest Level of Education
Trade School
|
7 Participants
n=342 Participants
|
13 Participants
n=343 Participants
|
20 Participants
n=685 Participants
|
|
Highest Level of Education
Missing/Not reported
|
2 Participants
n=342 Participants
|
3 Participants
n=343 Participants
|
5 Participants
n=685 Participants
|
|
Employment
Yes, Full Time
|
58 Participants
n=342 Participants
|
48 Participants
n=343 Participants
|
106 Participants
n=685 Participants
|
|
Employment
Yes, Part Time
|
40 Participants
n=342 Participants
|
35 Participants
n=343 Participants
|
75 Participants
n=685 Participants
|
|
Employment
No
|
242 Participants
n=342 Participants
|
257 Participants
n=343 Participants
|
499 Participants
n=685 Participants
|
|
Employment
Missing
|
2 Participants
n=342 Participants
|
3 Participants
n=343 Participants
|
5 Participants
n=685 Participants
|
|
Medication Assistance
No, I do it myself
|
320 Participants
n=342 Participants
|
310 Participants
n=343 Participants
|
630 Participants
n=685 Participants
|
|
Medication Assistance
Yes, from a healthcare professional
|
4 Participants
n=342 Participants
|
5 Participants
n=343 Participants
|
9 Participants
n=685 Participants
|
|
Medication Assistance
Yes, from a friend or family member
|
16 Participants
n=342 Participants
|
25 Participants
n=343 Participants
|
41 Participants
n=685 Participants
|
|
Medication Assistance
Missing
|
2 Participants
n=342 Participants
|
3 Participants
n=343 Participants
|
5 Participants
n=685 Participants
|
|
Charlson Comorbidity Index (CCI):
|
1.09 Scores on a Scale
STANDARD_DEVIATION 1.83 • n=342 Participants
|
1.23 Scores on a Scale
STANDARD_DEVIATION 1.92 • n=343 Participants
|
1.16 Scores on a Scale
STANDARD_DEVIATION 1.88 • n=685 Participants
|
PRIMARY outcome
Timeframe: Baseline, 6 months, 12 MonthsPopulation: Any discrepancies between the analysis population and the number of participants assigned to study arms are attributable to attrition; see the Participant Flow diagram for detailed accounting. Electronic records were available for participants who missed 6 and 12 but had not withdrawn from the study.
To calculate the Total Standardized Daily Dose (TSDD), we first calculated the Standardized Daily Dose (SDD) for each anticholinergic medication with an ACB Score of 2 or 3. SDD was calculated by multiplying the strength by the units per dose and frequency per day and number of refills. The product was divided by the minimum effective daily dose (where available) or the minimum effective geriatric dose to standardize the quantity across multiple classes of medications. The SDD for all anticholinergics with an ACB score 2 or 3 was then summed for each participant for each 6-month period, and divided by the number of days in the relevant six month period to arrive at a TSDD. Range: The minimum possible value is 0 (optimal outcome; indicating zero exposure to ACB 2 or 3 medications). There is no fixed theoretical maximum score(higher value more exposure), as the upper limit is mathematically determined by the total volume and combination of medications a participant is prescribed.
Outcome measures
| Measure |
Attention Control App
n=343 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=342 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Total Standardized Daily Dose (TSDD) - From Medical Records
Baseline
|
1.68 Standardized Doses Per Day
Standard Deviation 3.57
|
1.59 Standardized Doses Per Day
Standard Deviation 3.04
|
|
Total Standardized Daily Dose (TSDD) - From Medical Records
6 Months
|
1.19 Standardized Doses Per Day
Standard Deviation 3.53
|
0.86 Standardized Doses Per Day
Standard Deviation 1.61
|
|
Total Standardized Daily Dose (TSDD) - From Medical Records
12 Month
|
1.29 Standardized Doses Per Day
Standard Deviation 3.18
|
1.27 Standardized Doses Per Day
Standard Deviation 2.51
|
PRIMARY outcome
Timeframe: Baseline, 6, and 12 MonthsPopulation: Any discrepancies between the analysis population and the number of participants assigned to study arms are attributable to attrition; see the Participant Flow diagram for detailed accounting. Electronic records were available for participants who missed 6 and 12 but had not withdrawn from the study.
Construct: Measures natural log-transformed average daily exposure to medications with an Anticholinergic Cognitive Burden (ACB) score of 2 or 3 to normalize data distribution.How Computed: Medication Standardized Daily Dose (SDD) = (strength × units/dose × frequency/day × refills) / minimum effective daily or geriatric dose. The SDD for all eligible drugs is summed over 6 months, divided by the number of days in that period to find raw TSDD, and natural log-transformed ($\\ln(x+1)$ or similar) for the final score.Scale Range: Minimum value is 0 (representing 0 raw TSDD, or zero exposure). There is no fixed theoretical maximum, as it is mathematically determined by the volume of medications prescribed.Interpretation: A value of 0 is the optimal outcome (no exposure). Higher values represent greater exposure (worse outcome).
Outcome measures
| Measure |
Attention Control App
n=343 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=342 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Log Transformed Total Standardized Daily Dose (TSDD) - From Medical Records
Baseline
|
-1.12 ln(doses per day)
Standard Deviation 2.70
|
-0.93 ln(doses per day)
Standard Deviation 2.45
|
|
Log Transformed Total Standardized Daily Dose (TSDD) - From Medical Records
6 Months
|
-3.01 ln(doses per day)
Standard Deviation 3.52
|
-3.32 ln(doses per day)
Standard Deviation 3.50
|
|
Log Transformed Total Standardized Daily Dose (TSDD) - From Medical Records
12 Month
|
-2.69 ln(doses per day)
Standard Deviation 3.59
|
-3.04 ln(doses per day)
Standard Deviation 3.68
|
SECONDARY outcome
Timeframe: Baseline, 6 months, and 12 monthsPopulation: Any discrepancies between the analysis population and the number of participants assigned to study arms are attributable to attrition; see the Participant Flow diagram for detailed accounting.
An overall cognitive score evaluating three domains: memory/new learning, executive function, and processing speed. Calculated by taking the mean of standardized Z-scores from the following specific tests: Hopkins Verbal Learning Test-Revised (HVLT-R) total and delayed recall; Trail Making Test Parts A and B; Phonetic Fluency; Semantic Fluency (adjusted); and Symbol Digit Modalities Test (correct). A Z-score of 0 represents the baseline study population mean. Standardized scores theoretically range from -3.0 to +3.0. Higher positive Z-scores (standard deviations above the mean) represent better cognitive performance (better outcome). Lower negative Z-scores represent worse cognitive performance (worse outcome). No clinical threshold is defined. Z-scores were derived using baseline means, with timed tests (e.g., Trails) inverted prior to averaging so higher always means better performance.
Outcome measures
| Measure |
Attention Control App
n=342 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=340 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Overall Cognitive Score
Baseline
|
-0.02 Z-Scores
Standard Deviation 0.58
|
-0.01 Z-Scores
Standard Deviation 0.61
|
|
Overall Cognitive Score
6 Months
|
-0.12 Z-Scores
Standard Deviation 0.55
|
-0.09 Z-Scores
Standard Deviation 0.51
|
|
Overall Cognitive Score
12 Month
|
-0.10 Z-Scores
Standard Deviation 0.61
|
-0.05 Z-Scores
Standard Deviation 0.50
|
SECONDARY outcome
Timeframe: BaselinePopulation: Missing data
Computer-based assessment of Choice Reaction Time (CRT). It is used to evaluate executive function, attention, and psychomotor speed by measuring the time elapsed between the presentation of one of multiple possible stimuli and the participant's correct response. The final score represents the average response time (in milliseconds/seconds) across all valid test trials. The minimum value is 0. There is no fixed theoretical maximum, as the upper limit is bounded only by the participant's maximum delay. Lower values represent faster reaction times, indicating better executive functioning and psychomotor speed (a better outcome). Higher values indicate slower reaction times (a worse outcome).
Outcome measures
| Measure |
Attention Control App
n=243 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=247 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Choice Reaction Time (CRT)
|
52.86 Average Response Time (Seconds)
Standard Deviation 19.78
|
59.58 Average Response Time (Seconds)
Standard Deviation 15.83
|
SECONDARY outcome
Timeframe: Baseline, 6 months, and 12 monthsPopulation: Any discrepancies between the analysis population and the number of participants assigned to study arms are attributable to attrition; see the Participant Flow diagram for detailed accounting.
The Health Utilities Index Mark 3 (HUI3) is a self-reported, multi-attribute health status classification system used to measure overall health-related quality of life and functional capacity. The score is calculated using responses across eight dimensions of health (vision, hearing, speech, ambulation, dexterity, emotion, cognition, and pain). These subscales are combined using a mathematically weighted scoring algorithm to compute a single total utility index score. The total utility score ranges from a minimum of -0.36 (representing a health state considered worse than death) to a maximum of 1.00 (representing perfect health). A score of 0.00 represents death. Higher values represent a better health-related quality of life (a better outcome). Lower values represent worse health status (a worse outcome).
Outcome measures
| Measure |
Attention Control App
n=313 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=306 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Health Utilities Index (HUI) Mark 3
Baseline
|
0.63 Score on a Scale
Standard Deviation 0.32
|
0.63 Score on a Scale
Standard Deviation 0.31
|
|
Health Utilities Index (HUI) Mark 3
6 Months
|
0.60 Score on a Scale
Standard Deviation 0.31
|
0.61 Score on a Scale
Standard Deviation 0.31
|
|
Health Utilities Index (HUI) Mark 3
12 Month
|
0.63 Score on a Scale
Standard Deviation 0.31
|
0.60 Score on a Scale
Standard Deviation 0.33
|
SECONDARY outcome
Timeframe: Baseline, 6 months, and 12 monthsPopulation: Any discrepancies between the analysis population and the number of participants assigned to study arms are attributable to attrition; see the Participant Flow diagram for detailed accounting.
Hopkins Verbal Learning Test (HVLT) Total Recall. It is a paper-based list learning and recall assessment used to evaluate verbal memory and new learning capacity. Participants are read a list of 12 words and asked to freely recall as many as possible across three consecutive learning trials. The total recall score is calculated by summing the number of correctly recalled words across all three trials. The total recall score ranges from a minimum of 0 to a maximum of 36. Higher values represent a greater number of words correctly recalled, indicating better memory and verbal learning function (a better outcome). Lower scores indicate worse memory function (a worse outcome).
Outcome measures
| Measure |
Attention Control App
n=342 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=340 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Hopkins Verbal Learning Test (HVLT) Total Recall
Baseline
|
26.01 Raw Score
Standard Deviation 5.44
|
26.36 Raw Score
Standard Deviation 5.58
|
|
Hopkins Verbal Learning Test (HVLT) Total Recall
6 Months
|
25.35 Raw Score
Standard Deviation 5.24
|
26.18 Raw Score
Standard Deviation 5.24
|
|
Hopkins Verbal Learning Test (HVLT) Total Recall
12 Month
|
26.49 Raw Score
Standard Deviation 5.51
|
26.71 Raw Score
Standard Deviation 5.35
|
SECONDARY outcome
Timeframe: Baseline, 6 months, 12 monthsPopulation: Any discrepancies between the analysis population and the number of participants assigned to study arms are attributable to attrition; see the Participant Flow diagram for detailed accounting.
Hopkins Verbal Learning Test (HVLT) Delayed Recall. It is a paper-based assessment used to evaluate delayed verbal memory retention and recall capacity. After a standard delay interval (typically 20 to 25 minutes) following the initial learning trials, participants are asked to freely recall the original list of 12 words. The delayed recall score is the total number of words correctly recalled from memory. The score ranges from a minimum of 0 to a maximum of 12. Higher values represent a greater number of words retained and recalled after the delay, indicating better memory retention (a better outcome). Lower scores indicate worse memory retention (a worse outcome).
Outcome measures
| Measure |
Attention Control App
n=342 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=339 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Hopkins Verbal Learning Test (HVLT) Delayed Recall
Baseline
|
9.00 Raw Score
Standard Deviation 2.64
|
9.27 Raw Score
Standard Deviation 2.38
|
|
Hopkins Verbal Learning Test (HVLT) Delayed Recall
6 Months
|
8.65 Raw Score
Standard Deviation 2.62
|
9.06 Raw Score
Standard Deviation 2.41
|
|
Hopkins Verbal Learning Test (HVLT) Delayed Recall
12 Month
|
8.96 Raw Score
Standard Deviation 2.62
|
9.22 Raw Score
Standard Deviation 2.45
|
SECONDARY outcome
Timeframe: Baseline, 6 months, and 12 monthsPopulation: Any discrepancies between the analysis population and the number of participants assigned to study arms are attributable to attrition; see the Participant Flow diagram for detailed accounting.
Number Correct Line Segments. This is a performance-based metric derived from the Trail Making Test (TMT) used to assess visual search, scanning, processing speed, and executive function, particularly when a participant is unable to complete the full timed test. The score is calculated by counting the total number of correct line segments a participant successfully draws connecting the sequences of encircled numbers (or numbers and letters) within the allotted test parameters. The score ranges from a minimum of 0 to a maximum of 25. Higher values represent a greater number of correctly drawn segments, indicating better cognitive processing speed and executive functioning (a better outcome). Lower values indicate worse cognitive performance (a worse outcome).
Outcome measures
| Measure |
Attention Control App
n=341 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=339 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Trail Making Test (TMT) Parts A
Baseline
|
24.96 Number Correct Line Segments
Standard Deviation 0.29
|
24.91 Number Correct Line Segments
Standard Deviation 1.36
|
|
Trail Making Test (TMT) Parts A
6 Months
|
25 Number Correct Line Segments
Standard Deviation 0
|
25 Number Correct Line Segments
Standard Deviation 0
|
|
Trail Making Test (TMT) Parts A
12 Month
|
24.94 Number Correct Line Segments
Standard Deviation 0.91
|
25.00 Number Correct Line Segments
Standard Deviation 0
|
SECONDARY outcome
Timeframe: Baseline, 6 months, and 12 monthsPopulation: Any discrepancies between the analysis population and the number of participants assigned to study arms are attributable to attrition; see the Participant Flow diagram for detailed accounting.
Number Correct Line Segments (TMT Part B). This is a performance-based metric derived from the Trail Making Test Part B used to assess executive function, cognitive flexibility, and visual-motor tracking. It is particularly useful for quantifying performance when a participant is unable to complete the full timed test. The score is calculated by counting the total number of correct line segments a participant successfully draws connecting the 25 encircled numbers and letters in an alternating sequence (1, A, 2, B, 3, C...) within the allotted test parameters. The score ranges from a minimum of 0 to a maximum of 25. Higher values represent a greater number of correctly drawn segments, indicating better cognitive flexibility and executive functioning (a better outcome). Lower values indicate worse cognitive performance (a worse outcome).
Outcome measures
| Measure |
Attention Control App
n=337 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=336 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Trail Making Test (TMT) Parts B
Baseline
|
24.36 Number Correct Line Segments
Standard Deviation 2.53
|
24.29 Number Correct Line Segments
Standard Deviation 3.07
|
|
Trail Making Test (TMT) Parts B
6 Months
|
24.70 Number Correct Line Segments
Standard Deviation 1.25
|
24.72 Number Correct Line Segments
Standard Deviation 1.43
|
|
Trail Making Test (TMT) Parts B
12 Month
|
24.38 Number Correct Line Segments
Standard Deviation 2.49
|
24.70 Number Correct Line Segments
Standard Deviation 1.81
|
SECONDARY outcome
Timeframe: Baseline, 6 months, and 12 monthsPopulation: Any discrepancies between the analysis population and the number of participants assigned to study arms are attributable to attrition; see the Participant Flow diagram for detailed accounting.
Digit-Symbol Substitution Test (DSST), utilizing the Wechsler Adult Intelligence Scale-IV (WAIS-IV) Coding subtest. It is a paper-based assessment used to evaluate processing speed, visual-motor coordination, and sustained attention. Participants are provided a key pairing numbers (1 through 9) with simple geometric symbols. They are given a strict time limit (120 seconds) to draw the correct corresponding symbols beneath a series of randomized numbers. The final score is the total number of correctly drawn symbols within the time limit. The score ranges from a minimum of 0 to a maximum of 135 (the maximum possible items on the WAIS-IV Coding form). Higher values represent a greater number of correctly matched symbols, indicating faster processing speed and better cognitive performance (a better outcome). Lower scores indicate slower processing speed (a worse outcome).
Outcome measures
| Measure |
Attention Control App
n=312 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=308 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Digit-Symbol Substitution Test (DSST) Number of Correct Responses
Baseline
|
41.31 Score on a Scale
Standard Deviation 12.04
|
41.37 Score on a Scale
Standard Deviation 12.42
|
|
Digit-Symbol Substitution Test (DSST) Number of Correct Responses
6 Months
|
42.48 Score on a Scale
Standard Deviation 13.98
|
42.17 Score on a Scale
Standard Deviation 12.41
|
|
Digit-Symbol Substitution Test (DSST) Number of Correct Responses
12 Month
|
43.63 Score on a Scale
Standard Deviation 13.61
|
43.43 Score on a Scale
Standard Deviation 11.25
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 monthsPopulation: They were allowed to skip questions
Medication Perceptions Questionnaire. It is a 9-item survey developed in-house (adapted from Health Belief Model constructs and the revised Patients' Attitudes Towards Deprescribing Questionnaire) to assess participants' beliefs and attitudes regarding their medications and deprescribing. Participants rate items on a 5-point Likert agreement scale. The final score is calculated as a subscale average of the answered items (which allows for missing data if a participant skipped a question). The subscale average score ranges from a minimum of 1 to a maximum of 5. Higher scores indicate more disagreement (less agreement) with the survey statements. Lower scores indicate stronger agreement. The clinical favorability (better/worse outcome) depends on the specific construct of the subscale statement.
Outcome measures
| Measure |
Attention Control App
n=295 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=305 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Medication Perceptions
Threat awareness-susceptibility: If I regularly take certain medications...
|
3.3 Scores on a Scale
Standard Deviation 0.9
|
3.4 Scores on a Scale
Standard Deviation 1.0
|
|
Medication Perceptions
Cues to action: When I think about my medications...
|
1.9 Scores on a Scale
Standard Deviation 0.7
|
1.9 Scores on a Scale
Standard Deviation 0.7
|
|
Medication Perceptions
Perceived deprescribing benefit: If I stop taking certain medications...
|
3.0 Scores on a Scale
Standard Deviation 0.9
|
3.1 Scores on a Scale
Standard Deviation 0.8
|
|
Medication Perceptions
Perceived deprescribing barriers: When I think about changing my medications...
|
3.0 Scores on a Scale
Standard Deviation 0.9
|
3.0 Scores on a Scale
Standard Deviation 0.8
|
|
Medication Perceptions
Perceived self-efficacy: When I think about my medications...
|
2.2 Scores on a Scale
Standard Deviation 0.7
|
2.1 Scores on a Scale
Standard Deviation 0.7
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 monthsPopulation: Any discrepancies between the analysis population and the number of participants assigned to study arms are attributable to attrition; see the Participant Flow diagram for detailed accounting.
The Self-Reported Deprescribing Behavior Survey is an in-house, 4-item questionnaire designed to assess a participant's self-reported actions and behaviors related to stopping or reducing their medications (deprescribing). Item Scoring: Participants rate each of the 4 items individually using a 5-point Likert scale (1 = Strongly Agree, 5 = Strongly Disagree). Score Generation: The scores of the 4 individual items are mathematically averaged to calculate a single overall composite score. Scale Range: The overall composite average score ranges from a minimum of 1 to a maximum of 5. Outcome Direction: Lower overall average values (closer to 1) indicate stronger agreement with active deprescribing behaviors, which represents a better clinical outcome. Higher overall average values (closer to 5) indicate greater disagreement, which represents a worse clinical outcome.
Outcome measures
| Measure |
Attention Control App
n=295 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=305 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Self-reported Deprescribing Behavior
|
3.3 Scores on a Scale
Standard Deviation 0.8
|
3.2 Scores on a Scale
Standard Deviation 0.8
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 monthsPopulation: Any discrepancies between the analysis population and the number of participants assigned to study arms are attributable to attrition; see the Participant Flow diagram for detailed accounting.
Proportion of months out of the total study time the participant logged into the application at least once.
Outcome measures
| Measure |
Attention Control App
n=297 Participants
1\) Attention Control App provides a medication list for older patients to use, but lacks the conversation starters for patients to use with their physicians aimed at reducing exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
Brain Safe App
n=308 Participants
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
|---|---|---|
|
Technology Use-
|
0.34 Proportion of Months
Standard Deviation 0.29
|
0.36 Proportion of Months
Standard Deviation 0.29
|
Adverse Events
Brain Safe App
Attention Control App
Serious adverse events
| Measure |
Brain Safe App
n=342 participants at risk
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
Attention Control App
n=343 participants at risk
1\) Attention Control App provides a medication list for older patients to use but lacks the conversation starters for patient to use with there physicians aimed at reduction in exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
|---|---|---|
|
General disorders
Life Threatening
|
0.29%
1/342 • Number of events 1 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
0.58%
2/343 • Number of events 2 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
|
General disorders
Hospitalization
|
20.8%
71/342 • Number of events 138 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
22.2%
76/343 • Number of events 145 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
|
General disorders
Disability/Incapacity
|
3.5%
12/342 • Number of events 19 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
5.5%
19/343 • Number of events 28 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
|
General disorders
Other/Unspecified Serious AE
|
7.9%
27/342 • Number of events 39 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
6.4%
22/343 • Number of events 35 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
Other adverse events
| Measure |
Brain Safe App
n=342 participants at risk
1)Brain Safe App provides conversation starters for older adult patients on target anticholinergics. The conversation starters assist the patient to have discussions with their physicians regarding reduction in exposure to prescription anticholinergics. 2) Provides anticholinergic risk assessment.
|
Attention Control App
n=343 participants at risk
1\) Attention Control App provides a medication list for older patients to use but lacks the conversation starters for patient to use with there physicians aimed at reduction in exposure to prescription anticholinergics.2) No anticholinergic risk assessment.
|
|---|---|---|
|
General disorders
Non-serious AE - Mild
|
0.29%
1/342 • Number of events 1 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
0.29%
1/343 • Number of events 1 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
|
General disorders
Non-serious AE - Moderate
|
1.8%
6/342 • Number of events 6 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
2.9%
10/343 • Number of events 10 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
|
General disorders
Non-serious AE - Severe
|
0.88%
3/342 • Number of events 3 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
0.58%
2/343 • Number of events 2 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
|
General disorders
Non-serious AE - Severity not recorded
|
0.88%
3/342 • Number of events 3 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
0.87%
3/343 • Number of events 3 • From enrollement to completion of 12 month followup
Adverse event terms were recorded as free-text entries without standardized clinical coding. Because events often included mixed or non-specific symptom descriptions, organ system classifications were not derived from a controlled vocabulary. For structured reporting purposes, all events were assigned to a general organ system category.
|
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place