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NCT07016295Recruiting

Monitoring Arm Recovery After Stroke (MARS)

Developing an Accessible, Cost-Effective Motion Analysis Tool for Arm Movement After Stroke

Source: ClinicalTrials.gov · Last updated 11 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

People who have a stroke often find it hard to do the things they did before. This can be caused by problems with arm movement. One in five people do not get any arm movement back after a stroke. Arm movements can be measured accurately in a laboratory, but it is very expensive and not easy to do in hospital. That means it is hard to tell if the arm is recovering to move like it did before the stroke or adapting to perform tasks in other ways. To tell if a treatment is working, the investigators are making a phone app to record arm movement, using the camera. The recordings will be turned into data showing movement difficulties and sent to hospital records for clinicians. Clinicians will see if movement changes, to help choose the best treatment. The investigators are looking for twelve stroke survivors to help test this app. * The session will be at King's College London, on Guy's Campus. * It will run for 2-3 hours. * Participants will wear a vest or tight-fitting clothes. * The investigators will place non-invasive markers on the participants arm. * The investigators will video simple movements such as drinking from a cup. * The investigators will also measure the same simple movements using the laboratory cameras. This will show us if our app can measure arm movement as well as laboratory tests. If they do, the investigators will know the app is accurate. In future this technology can improve recovery by correcting stroke survivors when they perform home exercises.

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
30 May 2025
Start date
28 Jul 2025
Primary completion date
30 Sept 2026
Lead sponsor
King's College London
Diseases
Stroke
NCT number
NCT07016295

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 28 Jul 2025 to the primary completion date, 30 Sept 2026
  • 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.

Other illness

  • Severe cognitive impairment preventing ability to consent to treatment and understand and follow research protocol

Other

  • Severe language deficit preventing ability to consent to treatment and understand and follow research protocol
  • Shoulder pain \>3/10 on visual analog scale
  • Unable to maintain independent sitting balance without a high back support.
  • Wheelchair users that are unable to transfer with assistance of 1 to lab chair or whose wheelchair backrest cannot colapse.

Who the study is looking for

  • History of stroke
  • Arm impairment evidenced by Fugl-Meyer Upper Limb Assessment between 9-60/66.

Criteria the registry did not label

  • Stroke survivors

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre for Human and Applied Physiological Sciences
Coordinator of this site? Confirm its status
LondonUnited KingdomRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.