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Behavioural Intervention
Self-Management Program for Stroke Survivors (CHAMPS Trial)
N/A
Waitlist Available
Research Sponsored by University of New Mexico
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to improve the CHAMPS self-management program for stroke survivors. It will assess whether the program can help improve cardiovascular health, quality of life, self-confidence, and reduce the risk of
Who is the study for?
This trial is for adults over 18 who've had an ischemic stroke within the last 90 days. They should not have pre-stroke dementia, major depression, or recent drug/alcohol misuse. Participants need some executive function impairment but can't have severe aphasia. Access to video-conferencing tools is required.
What is being tested?
The CHAMPS intervention is being tested to see if it helps stroke survivors manage their health better and reduce risks like heart problems or another stroke. It aims to improve quality of life and self-confidence in managing health by teaching new skills through video conferencing.
What are the potential side effects?
Since CHAMPS involves cognitive strategies and skill learning via video-conference, there are no direct medical side effects; however, participants may experience frustration or fatigue during the learning process.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Battery of American Heart Association Life's Essential 8
Suitability and Feasibility Survey
Secondary study objectives
Healthcare utilization Questionnaire
NIH Stroke Scale
Stroke Specific Quality of Life Scale
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Feasibility ArmExperimental Treatment1 Intervention
A 10 sessions over 5 week virtual interaction between an occupational therapist and a person who is post-stroke, engage in meta-cognitive coaching to develop strategies to overcome barriers to daily living experienced in early stages of stroke. Outcomes anticipated are related to the American Heart Association's Healthy 8.
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Who is running the clinical trial?
University of New MexicoLead Sponsor
384 Previous Clinical Trials
3,525,948 Total Patients Enrolled
5 Trials studying Stroke
5,271 Patients Enrolled for Stroke
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