NCT07776392Completed
Occupational Therapy Instructmental Activities of Daily Living and Psychosocial Modules Program for Stroke Survivors
Occupational Therapy Instrumental Activities of Daily Living and Psychosocial Program for Healthy Habits and Role of Stroke Survivors
Source: ClinicalTrials.gov · Last updated 20 Aug 2026
Brief summary (registry, in English)
The study aims to recruit and enroll 25 participants who meet specific criteria, which will be communicated to potential participants, along with information about the study\'s goals, time commitments, benefits, and risks. Participants can ask questions and receive consent forms to review and sign. Once participants sign consent forms, the primary investigator will generate non-identifiable codes for each participant using an Excel spreadsheet to maintain confidentiality and protect participant identities. Participants will be randomly assigned to one of two groups to minimize potential bias and ensure that each group is representative of the overall population. One group will receive a psychosocial intervention, while the other group will engage in instrumental activities of daily living.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 19 (actual)
- First submitted
- 13 Aug 2026
- Start date
- Jan 2024
- Primary completion date
- May 2024
- Lead sponsor
- Texas Woman's University
- Diseases
- Stroke
- NCT number
- NCT07776392
What you commit to
- Study type: Interventional
- Participants enrolled: 19
- From Jan 2024 to the primary completion date, May 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Use of medications that may affect participant's level of consciousness or fatigue
Other
- Acute medical problems
- Presence of any contraindications, injuries, or surgeries
- Significant pain that interferes with participation in program activities
- Impaired cognition level: Participants will need to have normal cognition in order to understand the study procedure. Therefore, we will use the Mini-Mental State Exam (MMSE) survey, with a total score of 30, to screen cognition. If the score on the MMSE survey is less than 24, the participant will be excluded.
Who the study is looking for
- Be at least 18 years old;
- Have a history of unilateral stroke no less than 3 months and be medically stable prior to the study
- Be able to follow three-step commands
- Have a score equal to or less than 20 on the 9-question Patient Health Questionnaire for without depression
- Participants must commit to 8 weeks to participate in the full OT lifestyle redesign program
- Be able to speak and understand English, as the program and study materials are in English
- Internet access for zoom is required for participants
Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Texas Woman's University Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.