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Stroke survivors and staff team up to fix trial slip-ups

NCT ID NCT07484958

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study brings together stroke survivors, families, staff, and researchers to co-design a toolkit that helps everyone follow trial protocols in inpatient stroke rehabilitation. The goal is to reduce missed sessions and errors, making trial results more trustworthy. About 38 people will take part in surveys, interviews, and workshops to shape the toolkit.

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 create a practical toolkit that makes future stroke rehabilitation trials more reliable and effective.
What could go wrong
This is a small, early-stage co-design study with only 38 participants, so the toolkit may not work in all settings or improve adherence as hoped.

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 38 people

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

Started

Feb 2026

Expected to finish

Dec 2027

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

Stroke survivors, family member or friend of stroke survivor, stroke rehabilitation staff, healthcare leaders, stroke rehabilitation researchers, funders of stroke rehabilitation research.

Ages

18 years and older

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.

Participants will be eligible if they meet the following criteria: 8.1.1 Inclusion criteria stroke survivors * Adults (aged 18+) who have experienced a stroke. No time limit since stroke * Able to provide informed consent * Sufficient communication abilities (verbal or non-verbal, with or without support) to participate in co-design activities * Received inpatient stroke rehabilitation after their stroke * Has or has not previously participated in a stroke rehabilitation clinical trial during their hospital-based stroke rehabilitation * Willing to participate in co-design activities and share their perspectives. 8.1.2 Inclusion criteria family member/friend of stroke survivor * Adults (aged 18+) who are a family member, friend, or informal caregiver of a stroke survivor. * Able and willing to provide informed consent. * Willing to participate in co-design activities and share their perspectives. 8.1.3 Inclusion criteria stroke rehabilitation staff * Registered staff currently working in stroke rehabilitation who routinely prescribe and/or supporting stroke rehabilitation activities (e.g., physiotherapist, occupational therapist, rehabilitation nurses, rehabilitation physician) * ≥6 months of experience in hospital-based stroke rehabilitation settings * Employed in an organisation that provides NHS hospital-based stroke rehabilitation services * Willing to participate in co-design activities and share their perspectives. 8.1.4 Inclusion criteria healthcare leaders (e.g., Managers, Administrators, Policy Makers) * Individuals who are accountable and responsible for the operational, clinical, and/or strategic delivery of stroke rehabilitation, rehabilitation and/or therapy services within a NHS hospital * Individuals working in an Integrated Care Board with rehabilitation and/or research in their portfolio * Experience in implementing/influencing stroke rehabilitation policy/service delivery * Willing to participate in co-design activities and share their perspectives. 8.1.5 Inclusion criteria stroke rehabilitation researchers * Active researchers with experience in designing, conducting and evaluating stroke rehabilitation or physical rehabilitation research * Affiliated with academic or research institutions * Willing to participate in co-design activities and share their perspectives. 8.1.6 Inclusion criteria for funders * Currently employed, contracted to, or formally affiliated with a research funding organisation that reviews, commissions or funds stroke rehabilitation research (e.g., NIHR, Stroke Association, research councils, medical research councils, professional bodies or research charities) * Direct involvement in decision-making, monitoring or governance of stroke rehabilitation research within the past two years * Experience with funding processes related to stroke rehabilitation, rehabilitation or clinical trial oversight 8.2 Exclusion Criteria Participants will not be eligible if they meet any the following criteria: 8.2.1 Exclusion criteria for stroke survivors * Significant cognitive and/or communication impairment that preclude meaningful participation, even with support * Exhibiting aggression or other behaviour issues that put themselves and others at risk * Medical instability that would make participation unsafe or overly burdensome * Currently enrolled in another research study that could confound participation or data collection * Non-English speaking (research study does not offer language support). 8.2.2 Exclusion criteria for family member/friend of stroke survivor * Not family member or friend of a stroke survivor * Significant emotional distress or trauma that would be exacerbated by participation. * Non-English speaking (research study does not offer language support). 8.2.3 Exclusion criteria for stroke rehabilitation staff * Currently under disciplinary review or leave of absence. * ≤6 experience in NHS inpatient stroke rehabilitation * Inability to commit time to the study activities. 8.2.4 Exclusion criteria for healthcare leaders (e.g., Managers, Administrators, Policy Makers) * Not in a leadership or decision-making role within an organisation that provides NHS inpatient stroke rehabilitation or rehabilitation/therapy services * Not working in an Integrated Care Board/System * No experience in implementing or influencing stroke rehabilitation policy or service delivery * Conflict of interest with study funders or researchers. 8.2.5 Exclusion criteria for stroke rehabilitation researchers * No direct experience with stroke or rehabilitation research in the past two years. * No experience of hospital-based stroke or physical rehabilitation research in the past two years * Participation that would lead to conflicts of interest with the research team or funders. 8.2.6 Exclusion criteria for funders * Not employed by or formally affiliated with a research funding organisation that reviews, commissions or funds stroke rehabilitation research (e.g., NIHR, Stroke Association, research councils, medical research councils, professional bodies or research charities) * No direct involvement in decision-making, monitoring or governance of stroke rehabilitation research within the past two years * Conflict of interest with the research team or institutions delivering this study

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

How to take part

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

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. 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.

Contacts and locations

Locations

  • University of Plymouth, Faculty of Health

    Plymouth, Devon, PL4 6AB, United Kingdom

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