mCIMTModified Constraint-Induced Movement Therapy for Upper Limb Function in Stroke Patients
Conventional Physical Therapy
+ Modified Constraint Induced Movement Therapy
Brain Diseases+9
+ Cardiovascular Diseases
+ Central Nervous System Diseases
Treatment Study
Summary
Study start date: November 12, 2024
Actual date on which the first participant was enrolled.This study aims to explore how different types of physical therapy can improve arm and hand function, balance, and overall quality of life for people who have experienced a stroke and have long-term difficulties moving one side of their body. The researchers are particularly interested in comparing a special therapy called Modified Constraint-Induced Movement Therapy (mCIMT) and trunk restraint with regular physical therapy methods. Understanding which approach works best could lead to better rehabilitation strategies for stroke survivors, helping them regain more independence in their daily activities. Participants in the study will receive either conventional physical therapy or a combination of mCIMT and trunk restraint, along with conventional therapy. mCIMT involves limiting the use of the unaffected arm to encourage use of the affected arm, while trunk restraint helps with posture and balance. The study will measure improvements in arm and hand function, balance, and participants' quality of life. By evaluating these outcomes, the study seeks to determine which therapy method offers the most benefit to those recovering from a stroke.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.34 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 45 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
ExperimentalStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location