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Stroke patient movement linked to caregiver mental health

NCT ID NCT07504848

Knowledge-focused Sponsor: Ondokuz Mayıs 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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looks at how well stroke patients can move and how that affects the anxiety, depression, and burden of their caregivers. Researchers will assess 64 stroke patients and their family caregivers using mobility tests and mental health questionnaires. The goal is to understand the connection between patient mobility and caregiver well-being.

What this could mean

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

What this could lead to
If successful, this could help identify which stroke patients' mobility levels most impact caregiver mental health, guiding better support strategies.
What could go wrong
This is an observational study with only 64 participants, so results may not apply to all stroke patients or caregivers. It measures associations, not causes.

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.

Participants

About 64 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Apr 2026

An estimate. Start dates often move.

Expected to finish

Apr 2026

An estimate. End dates often move.

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.

Who is studied

This study includes adult individuals with a first-ever unilateral stroke and their primary caregivers. Stroke patients aged 18-75 years, at least 3 months post-stroke, with sufficient cognitive function (MMSE ≥24), and stable medical status are included. Caregivers are adults who have been living with the patient for at least one year and are the primary, non-professional caregivers.

Ages

18 to 75 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: 1. Stroke Patients: * Diagnosed with stroke according to WHO criteria (≥20% disability rate documented in Adult Disability Health Board Report) * Having a family member or relative who provides care * First-ever and unilateral stroke * Willing to participate voluntarily * Aged between 18-75 years * Post-stroke duration longer than 3 months * Stable vital signs * Scoring ≥24 on the Standardized Mini-Mental State Examination (SMMT) or the -Modified Mini-Mental State Examination for Illiterate Individuals (MMSE-E) * Able to understand and speak Turkish 2. Caregivers of Stroke Patients: * Willing to participate in the study * Living with the patient for at least 1 year * Being the primary (main responsible) caregiver and not receiving paid professional caregiving services * Aged 18 years or older * Scoring ≥24 on the Standardized Mini-Mental State Examination (SMMT) or MMSE-E Exclusion Criteria: 1. Stroke Patients: * Presence of severe comorbid conditions * Unwillingness to participate * History of multiple strokes * Bilateral hemiplegia * Presence of major neurological, orthopedic, or rheumatologic disorders affecting the musculoskeletal system other than stroke * Congenital anomalies or amputation causing disability * Uncontrolled arrhythmia, uncontrolled hypertension, or unstable cardiac conditions * Botulinum toxin injection within the last 6 months * Inability to establish cooperation * Presence of neglect, aphasia, or hemianopsia 2. Caregivers of Stroke Patients: * Unwillingness to participate * Living with the patient for less than 1 year * Presence of mental retardation, dementia, or severe psychotic disorders

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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.

Caregiver Stroke

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

More trials for these conditions

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