NCT06130891Completed
Effects of Cognitive Exercises With Sensory Motor Relearning Program on Upper Limb Function in Sub-Acute Stroke Patients
Source: ClinicalTrials.gov · Last updated 7 May 2024
Brief summary (registry, in English)
The goal of this clinical trial is to compare the effects of cognitive sensory motor relearning, and sensory-motor relearning program alone on manual ability, sensation, gross and fine movements, and cognition in post-stroke patients. The main aim is to evaluate the effectiveness of an integrated approach and its impact on motor function, sensory processing, and cognitive skills in sub-acute stroke patients, with the goal of contributing to the development of more efficient rehabilitation interventions for UL sensory-motor impairments after stroke.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 50 (actual)
- First submitted
- 9 Nov 2023
- Start date
- 5 Nov 2023
- Primary completion date
- 30 Mar 2024
- Lead sponsor
- Riphah International University
- Diseases
- Stroke
- NCT number
- NCT06130891
What you commit to
- Study type: Interventional
- Participants enrolled: 50
- From 5 Nov 2023 to the primary completion date, 30 Mar 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 who have severe visual or hearing impairments that would interfere with therapy or assessments.
Other illness
- Participants who have a history of significant neurological or psychiatric disorders, other than stroke, that could interfere with upper limb motor or sensory recovery.
- Participants who have other medical conditions that could interfere with therapy or assessments, such as severe arthritis or joint injuries.
Other
- Participants who are currently participating in another clinical trial or research study.
Who the study is looking for
- Both male and female patients.
- 45- 60 years of age.
- 1st ever stroke.
- Sub-acute ischemic stroke.
- 8-12 weeks post stroke patients.
- Participants must have motor and somatosensory deficits in the upper limb on the affected side, as indicated by an ARAT score between 40 and 50 out of 57.
- Participants must be able to provide informed consent or have a legal representative who can provide informed consent on their behalf.
- MoCA score between 18-24
- Modified Ashworth scale \< +1
Age in the registry: 45 years to 60 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 |
|---|---|---|---|
| THQ Hospital, Muridke, Sheikhupura, Punjab Coordinator of this site? Confirm its status | Sheikhupura | Pakistan | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.