Perturbation-induced Balance Training for Post-Stroke Individuals
Balance training
Brain Diseases+4
+ Cardiovascular Diseases
+ Central Nervous System Diseases
Treatment Study
Summary
Study start date: January 22, 2019
Actual date on which the first participant was enrolled.This study focuses on improving balance in individuals who have experienced a stroke. It uses a unique method called perturbation-induced reactive standing balance training. This involves applying gentle, unexpected disturbances to help participants improve their balance reactions. The study is important because it aims to enhance the quality of life for stroke survivors by reducing the risk of falls and improving mobility. During the study, participants will wear a belt connected to a mechanical weight drop system. This system will apply small, sudden pulls to challenge their balance. Participants will be asked to respond naturally, using their more affected leg to maintain balance. The study will measure the frequency of using the affected leg for balance, the time it takes to initiate a step, and the ability to regain balance after a lean. These measurements will be taken before and after the training sessions. The training will consist of 6 sessions within a three-week period, each lasting about an hour. Safety measures, such as a harness and rest breaks, will be provided to ensure participants' well-being.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.13 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 21 to 80 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.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary 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