Strengthening in Sub-acute Stroke Survivors: A Randomized Controlled Trial

Status Recruiting

Clinical Trial Summary

The goal of this study is to compare between Eccentric training and conventional therapy in sub-acute stroke survivors. The primary objective of this study is to evaluate improvements in gait speed after four months of ET in comparison to conventional therapy for patients with sub-acute stroke. Secondary objectives involve assessing: i) modifications in neuromuscular parameters of PF, ii) changes in muscle stiffness within PF during passive mobilization and active force generation, and iii) modifications in architectural parameters of PF.

Clinical Trial Description

This study will be a single-blinded, controlled, randomized design, wherein participants will be randomly assigned to one of two groups: the Conventional Therapy Group (CTG) or the Eccentric Training Group (ETG). Both groups will undergo a comprehensive series of assessments at three key time points: Ji (initial assessment), Jint (intermediate assessment), and Jf (final assessment). The study will commence with a recruitment phase, followed by a screening phase. Subsequently, there will be a 4-week period allocated for experimental testing before the intervention, and an additional 4 weeks for experimental testing after the intervention. These assessments will encompass a wide range of evaluations, including clinical health assessments, biomechanical assessments, neuromuscular evaluations, and functional assessments ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06140381
Study type	Interventional
Source	Clinique Du Parc de Belleville
Contact	belghith kalthoum, Investigator
Phone	0649260709
Email	belghith.kalthoum@gmail.com
Status	Recruiting
Phase	N/A
Start date	December 1, 2023
Completion date	October 1, 2024

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See also
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