NCT06739902Active, not recruiting
Comparing the Effectiveness of Traditional Physiotherapy Combined With Virtual Reality for Post-Stroke Patients
Source: ClinicalTrials.gov · Last updated 18 Dec 2024
Brief summary (registry, in English)
This study aims to evaluate the effectiveness of combining virtual reality (VR) therapy with traditional physiotherapy in post-stroke rehabilitation. Post-stroke patients often suffer from impairments in motor function, balance, and overall quality of life. While traditional physiotherapy is a widely accepted method for stroke recovery, incorporating VR technology may enhance treatment outcomes by providing an engaging, immersive environment that motivates patients to perform therapeutic movements.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 24 (actual)
- First submitted
- 13 Dec 2024
- Start date
- 28 Feb 2024
- Primary completion date
- 1 Aug 2024
- Lead sponsor
- Superior University
- Diseases
- Stroke
- NCT number
- NCT06739902
What you commit to
- Study type: Interventional
- Participants enrolled: 24
- From 28 Feb 2024 to the primary completion date, 1 Aug 2024
- 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.
Prior treatment
- Participants receiving rehabilitation or rigorous physical treatment in the previous three months were excluded.
Other illness
- Existence of additional neurological disorders (such as multiple sclerosis or Parkinson's disease) or serious medical conditions that could prevent participants from participating in the study.
Other
- Pregnant women or breastfeeding women.
- Participants who refused to participate in the study or provide informed consent.
Who the study is looking for
- Stroke, either ischemic or hemorrhagic
- Participants who can ambulate independently or with minimal assistance.
- Participants who were willing \& able to adhere to the study protocol.
- Including participants who were attending follow-up appointments \& completing outcome measures.
- Participants who were able to understand \& provide written informed consent
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Services Hospital, Shadman 1 Coordinator of this site? Confirm its status | Lahore | Pakistan | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.