University of Rochester Wilmot Cancer Institute
Rochester, New York, 14620, United States
NCT Number: NCT05775991
To gather key stakeholder input for feedback on the adaption of the COACH GA intervention (i.e., develop COACH-Cog) to enhance triadic communication among oncologists, care partners and patients with ADRD.
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Observational
Rochester, New York, 14620, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion/Exclusion Criteria:
The inclusion and exclusion criteria for participants are that they must be able to consent for themselves and must speak English.
For the medical oncologist focus group, participants must be a medical oncologist.
For the clinicians with expertise in cognitive impairment and dementia focus group, participants must be a clinician that treats patients with cognitive impairment and dementia.
For the older patients with cancer focus group, participants must be older than 65 years of age and have or had cancer.
For the caregivers of patients with dementia focus group, participants must be caregivers of patients with dementia or cognitive impairment.
Time frame: Through study completion approximately 3 months
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.
University of Rochester
Other
Enhancing Triadic Communication About Cognition for Older Adults With Alzheimer's Disease or Related Dementias Facing a Cancer Management Decision - Focus Groups
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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