HABIT intervention to improve hand use after stroke
Feasibility and Efficacy of HABIT - a Novel Occupational Therapy Intervention for Enhancing Daily-Use of the Affected Upper Extremity Among Individuals Post Stroke.
This study tests a new program to help people who have had a stroke use their affected hand more in daily activities by boosting their confidence and problem-solving skills.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 18 Years to 100 Years |
| Sex | All |
| Sponsor | Tel Aviv University Academic / other |
| Locations | 1 site (Tel Aviv) |
| Trial ID | NCT06455241 on ClinicalTrials.gov |
What this trial studies
This study evaluates the feasibility and initial effectiveness of the Hand Activities Behavior Intervention (HABIT) designed to enhance daily hand use in individuals who have experienced a stroke. The intervention focuses on improving non-motor components such as self-efficacy and frustration tolerance through group discussions, problem-solving, and practice activities. Assessments will be conducted at four time points: baseline, pre-intervention, post-intervention, and follow-up via phone. The goal is to encourage the use of the affected upper extremity in everyday tasks.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and above, Hebrew speakers, with mild upper extremity motor impairment and no significant cognitive decline, living independently post-stroke.
Not a fit: Patients with other neurological conditions, significant proprioception deficits, or those with moderate to severe cognitive decline may not benefit from this intervention.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the daily hand use and overall quality of life for stroke survivors.
How similar studies have performed: Other studies have shown promise in using behavioral interventions to enhance motor function post-stroke, suggesting that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults aged 18 and above residing in their own homes * Hebrew speakers * Up to 10 years post-stroke * Mild upper extremity motor impairment but still report difficulty using their hand. This will be determined by a total score of 43/66, including the Hand subtest score of 7/14 points of the Fugl-Meyer Motor Assessment. * No significant cognitive decline (score of 19 and above on Montreal Cognitive Assessment) * Able to walk with or without assistive devices * Able to provide informed consent by signing a consent form * Full function of both hands and independent in daily function prior to stroke Exclusion Criteria: * Other neurological conditions or psychiatrists * with moderate or significant proprioception deficit (Thumb Localization Test \>1)
Where this trial is running
Tel Aviv
- Tel-Aviv University — Tel Aviv, Israel (Recruiting)
Study contacts
- Principal investigator: Debbie Rand — Tel Aviv University
- Study coordinator: Debbie Rand
- Email: drand@tauex.tau.ac.il
- Phone: +972-549490715
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.