Trial Outcomes & Findings for Cognitive Priming for Stroke Tele-rehabilitation (NCT NCT06555302)

NCT ID: NCT06555302

Last Updated: 2026-05-14

Results Overview

Montreal Cognitive Assessment (MoCA) is a 16-item objective cognitive screening measure. Total scores range from 0-30 points, with higher scores indicating better cognition.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

20 participants

Primary outcome timeframe

From pre-treatment assessment to post-treatment assessment, up to approximately 10 weeks

Results posted on

2026-05-14

Participant Flow

Participants were recruited from the MUSC Stroke Recovery Research Center's Registry for Stroke Recovery (RESTORE). They were recruited between 8/7/2024 and 2/12/2025. The first participant was enrolled on 8/20/2024 and the last participant was enrolled on 2/12/2025.

Of the 37 participants assessed for eligibility, 2 did not meet inclusion criteria, 1 declined to participate, and 14 were excluded for other reasons. 20 participants were assigned to treatment.

Participant milestones

Participant milestones
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Overall Study
STARTED
20
Overall Study
COMPLETED
19
Overall Study
NOT COMPLETED
1

Reasons for withdrawal

Reasons for withdrawal
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Overall Study
Withdrawal by Subject
1

Baseline Characteristics

PROMIS Sleep Disturbance is an 8-item self-report measure of perceived difficulties falling and/or staying asleep. Items are rated on a 5-point rating scale (1=no problem, 5=very much a problem). The summed raw score is converted into a normed T-score (mean=50, SD=10). Higher T-scores reflect more sleep disturbance.

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
n=20 Participants
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Age, Continuous
57.6 years
STANDARD_DEVIATION 12 • n=1512 Participants
Sex: Female, Male
Female
10 Participants
n=1512 Participants
Sex: Female, Male
Male
10 Participants
n=1512 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=1512 Participants
Race (NIH/OMB)
Asian
0 Participants
n=1512 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
1 Participants
n=1512 Participants
Race (NIH/OMB)
Black or African American
5 Participants
n=1512 Participants
Race (NIH/OMB)
White
13 Participants
n=1512 Participants
Race (NIH/OMB)
More than one race
0 Participants
n=1512 Participants
Race (NIH/OMB)
Unknown or Not Reported
1 Participants
n=1512 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants
n=1512 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
19 Participants
n=1512 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
n=1512 Participants
Montreal Cognitive Assessment (MoCA)
23.7 score on scale
STANDARD_DEVIATION 3.7 • n=1512 Participants
Patient Specific Functional Scale (PSFS)
2.2 score on scale
STANDARD_DEVIATION 1.6 • n=1512 Participants
Patient Health Questionnaire (PHQ-9)
5.4 score on scale
STANDARD_DEVIATION 4.9 • n=1512 Participants
NeuroQoL-Cognitive Function
46.6 t-score
STANDARD_DEVIATION 11.0 • n=1512 Participants
Performance Quality Rating Scale (PQRS)
6.1 score on scale
STANDARD_DEVIATION 2.7 • n=1512 Participants
Stroke Self Efficacy Questionnaire (SSEQ)
94.8 score on scale
STANDARD_DEVIATION 30.5 • n=1512 Participants
Inventory of Psychosocial Functioning (IPF)
21.0 score on scale
STANDARD_DEVIATION 11.1 • n=1512 Participants
PROMIS Sleep Disturbance
49.7 t-score
STANDARD_DEVIATION 15.2 • n=1512 Participants • PROMIS Sleep Disturbance is an 8-item self-report measure of perceived difficulties falling and/or staying asleep. Items are rated on a 5-point rating scale (1=no problem, 5=very much a problem). The summed raw score is converted into a normed T-score (mean=50, SD=10). Higher T-scores reflect more sleep disturbance.

PRIMARY outcome

Timeframe: From pre-treatment assessment to post-treatment assessment, up to approximately 10 weeks

Population: This includes only participants with both pre- and post-treatment data.

Montreal Cognitive Assessment (MoCA) is a 16-item objective cognitive screening measure. Total scores range from 0-30 points, with higher scores indicating better cognition.

Outcome measures

Outcome measures
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
n=19 Participants
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Change From Baseline in Global Cognition, as Measured by the Montreal Cognitive Assessment (MoCA)
1.74 total score
Standard Deviation 2.73

PRIMARY outcome

Timeframe: From pre-treatment assessment to post-treatment assessment, up to approximately 10 weeks

Population: This includes only participants with both pre- and post-treatment data.

The Patient Specific Functional Scale (PSFS) is a patient-reported measure of task-goal identification and difficulty performing the task on a 0-10-point ordinal scale with higher ratings indicating greater satisfaction with task performance.

Outcome measures

Outcome measures
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
n=19 Participants
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Change From Baseline Functional Task Performance and Activity Participation, as Measured by the Patient Specific Functional Scale (PSFS)
2.84 score on scale
Standard Deviation 2.05

PRIMARY outcome

Timeframe: From pre-treatment assessment to post-treatment assessment, up to approximately 10 weeks

Population: This includes only participants with both pre- and post-treatment data.

The Patient Health Questionnaire (PHQ-9) is a 9-item self-report measure of depression. Items query mood (feeling down, lack of interest), thoughts (guilt, suicidality), and physical symptoms (appetite, sleep, fatigue, concentration, restlessness). Each item is scored on a 4-point scale reflecting how often the symptom has occurred over the last 2 weeks (0=not at all, 3=nearly every day). Scores are summed (out of 27), with higher scores indicating more symptoms of depression.

Outcome measures

Outcome measures
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
n=19 Participants
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Change From Baseline Psychosocial Function (Depression), as Measured by the Patient Health Questionnaire (PHQ-9)
-0.26 score on scale
Standard Deviation 5.61

SECONDARY outcome

Timeframe: From pre-treatment assessment to post-treatment assessment, up to approximately 10 weeks

Population: This includes only participants with both pre- and post-treatment data.

The NeuroQoL-Cognitive Function Short Form v.2.0 is a 29-item subjective measure of cognitive function. This patient-reported outcome assesses perceived abilities in memory, attention, decision making, or in the application of such abilities to everyday tasks (e.g., planning, organizing, calculating, remembering, and learning) on a 5-item rating scale (1=cannot do to 5=no difficulty). The summed raw score is converted into a normed T-score (mean=50, SD=10). Higher T-scores reflect better perceived cognitive function.

Outcome measures

Outcome measures
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
n=19 Participants
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Change From Baseline Subjective Cognition, as Measured by the NeuroQoL-Cognitive Function
0.78 t-score
Standard Deviation 8.59

SECONDARY outcome

Timeframe: From intervention session #5 to intervention session #13 (approximately 5 weeks)

Population: This includes only participants with both pre- and post-treatment data.

The Performance Quality Rating Scale (PQRS) is a therapist-rated measure. The OT observes the participant's performance of a specific task and rates it on a 0-10-point ordinal scale, with higher ratings indicating greater task performance skill.

Outcome measures

Outcome measures
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
n=19 Participants
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Change From Baseline Functional Task Performance and Activity Participation, as Measured by the Performance Quality Rating Scale (PQRS)
0.53 score on scale
Standard Deviation 0.70

SECONDARY outcome

Timeframe: From pre-treatment assessment to post-treatment assessment, up to approximately 10 weeks

Population: This includes only participants with both pre- and post-treatment data.

The Stroke Self Efficacy Questionnaire (SSEQ) is a 13-item self-report measure of confidence (0-10-point Likert scale with higher numbers indicating greater confidence) doing at-home tasks such as using both hands to eat food or prepare a meal for oneself. Item scores are summed and total range from 0-130, with higher scores indicating greater self-efficacy.

Outcome measures

Outcome measures
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
n=19 Participants
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Change From Baseline Functional Task Performance and Activity Participation, as Measured by the Stroke Self Efficacy Questionnaire (SSEQ)
6.79 score on scale
Standard Deviation 18.20

SECONDARY outcome

Timeframe: From pre-treatment assessment to post-treatment assessment, up to approximately 10 weeks

Population: This includes only participants with both pre- and post-treatment data.

The Inventory of Psychosocial Functioning (IPF) is an 80-item self-report measure of impairment in 7 psychosocial domains within the last 30 days: romantic relationships, family, work, friendships and socializing, parenting, education, and self-care. Participants rate the frequency of difficulty on each item on a 7-point scale (0=never, 6=always). Scores are averaged by domain (if ≥80% of items are complete) and multiplied by 100; an overall score (grand mean) is the average of completed domain scores; higher scores indicate greater impairment in psychosocial function.

Outcome measures

Outcome measures
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
n=19 Participants
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Change From Baseline Psychosocial Function (Global), as Measured by the Inventory of Psychosocial Functioning (IPF)
-1.32 score on scale
Standard Deviation 10.92

SECONDARY outcome

Timeframe: From pre-treatment assessment to post-treatment assessment, up to approximately 10 weeks

Population: This includes only participants with both pre- and post-treatment data.

PROMIS Sleep Disturbance is an 8-item self-report measure of perceived difficulties falling and/or staying asleep. Items are rated on a 5-point rating scale (1=no problem, 5=very much a problem). The summed raw score is converted into a normed T-score (mean=50, SD=10). Higher T-scores reflect more sleep disturbance.

Outcome measures

Outcome measures
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
n=19 Participants
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Change From Baseline Psychosocial Function (Sleep), as Measured by the PROMIS Sleep Disturbance
-2.58 t-score
Standard Deviation 11.98

Adverse Events

Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)

Serious events: 0 serious events
Other events: 6 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Other adverse events
Measure
Cognitive Rehabilitation + Occupational Therapy (Telerehabilitation)
n=20 participants at risk
A trained OT will deliver the 8-week stroke telerehabilitation program. There will be 13 total sessions with 2 sessions/week for the first 5 weeks and 1 session/week for the last 3 weeks. The cognitive rehabilitation and OT components will be titrated as follows: * Sessions 1-4 will focus on cognitive rehab. * Sessions 5-10 will review/provide additional cognitive rehab and deliver OT. * Sessions 11-13 may briefly review cognitive rehab but focus primarily on OT.
Musculoskeletal and connective tissue disorders
Elbow pain
10.0%
2/20 • Number of events 2 • From enrollment until post-treatment assessment at the end of the study (approximately 10 weeks).
In this study, other (i.e., non-serious) adverse events were defined as those that were 1) unexpected, 2) related or possibly related to study participation, AND 3) severe or more prevalent than expected, in accordance with our local Institutional Review Board (IRB).
Injury, poisoning and procedural complications
Laceration
5.0%
1/20 • Number of events 1 • From enrollment until post-treatment assessment at the end of the study (approximately 10 weeks).
In this study, other (i.e., non-serious) adverse events were defined as those that were 1) unexpected, 2) related or possibly related to study participation, AND 3) severe or more prevalent than expected, in accordance with our local Institutional Review Board (IRB).
Surgical and medical procedures
Dental procedure
5.0%
1/20 • Number of events 1 • From enrollment until post-treatment assessment at the end of the study (approximately 10 weeks).
In this study, other (i.e., non-serious) adverse events were defined as those that were 1) unexpected, 2) related or possibly related to study participation, AND 3) severe or more prevalent than expected, in accordance with our local Institutional Review Board (IRB).
General disorders
Dizziness
5.0%
1/20 • Number of events 1 • From enrollment until post-treatment assessment at the end of the study (approximately 10 weeks).
In this study, other (i.e., non-serious) adverse events were defined as those that were 1) unexpected, 2) related or possibly related to study participation, AND 3) severe or more prevalent than expected, in accordance with our local Institutional Review Board (IRB).
Injury, poisoning and procedural complications
Bruise
5.0%
1/20 • Number of events 1 • From enrollment until post-treatment assessment at the end of the study (approximately 10 weeks).
In this study, other (i.e., non-serious) adverse events were defined as those that were 1) unexpected, 2) related or possibly related to study participation, AND 3) severe or more prevalent than expected, in accordance with our local Institutional Review Board (IRB).

Additional Information

Dr. Stephanie Aghamoosa

Medical University of South Carolina

Phone: 843-792-2956

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place