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Rebuilding life after stroke: can occupational therapy restore daily independence?

NCT ID NCT07776392

Symptom relief Sponsor: Texas Woman's University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time

Summary

This trial tests whether an 8-week occupational therapy program can help stroke survivors improve their ability to perform everyday tasks and adopt healthier habits. Participants are randomly assigned to either a psychosocial support group or a group focused on instrumental activities of daily living (IADL), such as managing finances or using transportation. The program involves weekly in-person group sessions lasting about 45 minutes. The study measures changes in participants' satisfaction and performance in daily activities, as well as their knowledge of healthy habits and roles.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
An 8-week occupational therapy program combining instrumental activities of daily living (IADL) training with psychosocial support, delivered in group sessions.
What this could lead to
If effective, this program could offer a structured way to help stroke survivors regain independence and improve their daily functioning and well-being.
What could go wrong
This is a small, early-stage trial, so results may not apply broadly. The program's success depends on participant engagement and may not outperform standard care.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

19 people

The number who actually took part.

Started

Jan 2024

Finished

May 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 99 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria * 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 Exclusion criteria listed. * Acute medical problems * Presence of any contraindications, injuries, or surgeries * Significant pain that interferes with participation in program activities * Use of medications that may affect participant's level of consciousness or fatigue * 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.

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Conditions

The condition(s) this trial relates to.

stroke disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Stroke

Contacts and locations

Locations

  • Texas Woman's University

    Dallas, Texas, 75235-7200, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.