Trial Outcomes & Findings for COACH-Cog Intervention Adaptation Focus Groups (NCT NCT05775991)
NCT ID: NCT05775991
Last Updated: 2024-12-11
Results Overview
Qualitative data gathered from participants during focus group participation. Focus groups will be audio-recorded and transcribed. Transcribed audio-recordings will be qualitatively analyzed for positive regard for the intervention and opportunities and recommendations for further intervention adaptation. Open coding using content analysis framework will be utilized for qualitative analysis.
Recruitment status
COMPLETED
Target enrollment
18 participants
Primary outcome timeframe
Through study completion approximately 3 months
Results posted on
2024-12-11
Participant Flow
Participant milestones
| Measure |
Medical Oncologists and Clincians
Individuals practicing as medical oncologists or with expertise in medical oncology. Clinicians with expertise in cognitive impairment and dementia.
|
Older Patients With Cancer
Older patients with cancer or older survivors of patients with cancer
|
Caregivers of Patients With Dementia or Cognitive Impairment
Caregivers of patients with dementia or cognitive impairment
|
|---|---|---|---|
|
Overall Study
STARTED
|
5
|
4
|
9
|
|
Overall Study
COMPLETED
|
5
|
4
|
7
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
2
|
Reasons for withdrawal
| Measure |
Medical Oncologists and Clincians
Individuals practicing as medical oncologists or with expertise in medical oncology. Clinicians with expertise in cognitive impairment and dementia.
|
Older Patients With Cancer
Older patients with cancer or older survivors of patients with cancer
|
Caregivers of Patients With Dementia or Cognitive Impairment
Caregivers of patients with dementia or cognitive impairment
|
|---|---|---|---|
|
Overall Study
Withdrawal by Subject
|
0
|
0
|
2
|
Baseline Characteristics
COACH-Cog Intervention Adaptation Focus Groups
Baseline characteristics by cohort
| Measure |
Medical Oncologists and Clinicians
n=5 Participants
Individuals practicing as medical oncologists or with expertise in medical oncology. Clinicians with expertise in cognitive impairment and dementia.
|
Older Patients With Cancer
n=4 Participants
Older patients with cancer or older survivors of patients with cancer
|
Caregivers of Patients With Dementia or Cognitive Impairment
n=9 Participants
Caregivers of patients with dementia or cognitive impairment
|
Total
n=18 Participants
Total of all reporting groups
|
|---|---|---|---|---|
|
Age, Customized
<=18 years
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
|
Age, Customized
Between 18 and 65 years Between 18 and 65 years Between 18 and 65 years Between 18 and 65 years
|
4 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
4 Participants
n=206 Participants
|
8 Participants
n=7 Participants
|
|
Age, Customized
>=65 years
|
0 Participants
n=99 Participants
|
4 Participants
n=107 Participants
|
5 Participants
n=206 Participants
|
9 Participants
n=7 Participants
|
|
Age, Customized
Unknown/Missing
|
1 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
1 Participants
n=7 Participants
|
|
Sex/Gender, Customized
Female
|
3 Participants
n=99 Participants
|
2 Participants
n=107 Participants
|
6 Participants
n=206 Participants
|
11 Participants
n=7 Participants
|
|
Sex/Gender, Customized
Male
|
1 Participants
n=99 Participants
|
2 Participants
n=107 Participants
|
2 Participants
n=206 Participants
|
5 Participants
n=7 Participants
|
|
Sex/Gender, Customized
Intersex
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
|
Sex/Gender, Customized
None of these describe me
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
|
Sex/Gender, Customized
Prefer not to answer
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
1 Participants
n=206 Participants
|
1 Participants
n=7 Participants
|
|
Sex/Gender, Customized
Missing
|
1 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
1 Participants
n=7 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
2 Participants
n=206 Participants
|
2 Participants
n=7 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
4 Participants
n=99 Participants
|
4 Participants
n=107 Participants
|
6 Participants
n=206 Participants
|
14 Participants
n=7 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
1 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
1 Participants
n=206 Participants
|
2 Participants
n=7 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
|
Race (NIH/OMB)
Asian
|
2 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
2 Participants
n=7 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
|
Race (NIH/OMB)
Black or African American
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
|
Race (NIH/OMB)
White
|
2 Participants
n=99 Participants
|
4 Participants
n=107 Participants
|
7 Participants
n=206 Participants
|
13 Participants
n=7 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
1 Participants
n=206 Participants
|
1 Participants
n=7 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
1 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
1 Participants
n=206 Participants
|
2 Participants
n=7 Participants
|
PRIMARY outcome
Timeframe: Through study completion approximately 3 monthsQualitative data gathered from participants during focus group participation. Focus groups will be audio-recorded and transcribed. Transcribed audio-recordings will be qualitatively analyzed for positive regard for the intervention and opportunities and recommendations for further intervention adaptation. Open coding using content analysis framework will be utilized for qualitative analysis.
Outcome measures
| Measure |
Medical Oncologists and Clinicians
n=5 Participants
Individuals practicing as medical oncologists or with expertise in medical oncology. Clinicians with expertise in cognitive impairment and dementia.
|
Older Patients With Cancer
n=4 Participants
Older patients with cancer or older survivors of patients with cancer
|
Caregivers of Patients With Dementia or Cognitive Impairment
n=9 Participants
Caregivers of patients with dementia or cognitive impairment
|
|---|---|---|---|
|
Qualitative Analysis of Focus Group Audio-recording Transcripts. Open Coding Using Content Analysis Framework Will be Utilized to Assess Positive Regard for the Intervention and Potential Intervention Adaptations.
Positive Quote Given
|
4 Participants
|
3 Participants
|
4 Participants
|
|
Qualitative Analysis of Focus Group Audio-recording Transcripts. Open Coding Using Content Analysis Framework Will be Utilized to Assess Positive Regard for the Intervention and Potential Intervention Adaptations.
Negative Quote Given
|
0 Participants
|
0 Participants
|
0 Participants
|
|
Qualitative Analysis of Focus Group Audio-recording Transcripts. Open Coding Using Content Analysis Framework Will be Utilized to Assess Positive Regard for the Intervention and Potential Intervention Adaptations.
No Quote Given Applicable
|
1 Participants
|
1 Participants
|
3 Participants
|
|
Qualitative Analysis of Focus Group Audio-recording Transcripts. Open Coding Using Content Analysis Framework Will be Utilized to Assess Positive Regard for the Intervention and Potential Intervention Adaptations.
Withdrew
|
0 Participants
|
0 Participants
|
2 Participants
|
Adverse Events
Medical Oncologists and Clinicians
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Older Patients With Cancer
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Caregivers of Patients With Dementia or Cognitive Impairment
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place