Clinical Trials Logo

Clinical Trial Summary

Stroke is a major health problem and can cause long-term disability. Among these sequelae, there are balance and mobility disorders, but also a higher rate of anxiety or depression disorders. This impairments impact activity of daily living, and social reintegration. That why the investigators need to explore options for long-term sustainable interventions that which takes into account the patient as a whole. In particular, regular physical activity is recommended, but it must be adaptable to the patient's impairments. Teaching yoga may be an interesting option. Indeed, yoga is a mind-body practice which become increasingly widespread in the world. Recent studies highlight positive effect of yoga for this population. However, accessibility to yoga classes can be limited by many factors: lack of transportation, lack of available health professionals, confinement requirements... Therefore, it seems relevant to evaluate the effectiveness of yoga delivered through tele-rehabilitation. The main objective of this study is to evaluate the effectiveness of a tele-yoga program adapted to stroke survivors to improve their functional balance. The secondary objectives are to evaluate the effectiveness of the adapted tele-yoga program in improving functional mobility, anxiety, depression and reintegration into normal life.


Clinical Trial Description

The investigators will conduct a single-blind randomised controlled trial to study the effectiveness of a tele-yoga programme compared to an inactive control group in improving balance in chronic post-stroke subjects. The primary hypothesis is that yoga is effective in improving balance in chronic post-stroke patients. The secondary hypothesis is that yoga is effective in improving functional mobility, anxiety, depression, and reintegration into normal life. The experiment will take place in metropolitan France, and the whole experimental procedure (recruitment, evaluation, experimentation) will take place at a distance, via information and communication technologies. The statistical power study indicates that 15 patients per group would be required. Subjects will be randomly assigned to one of the following groupe: the TELEYOG'AVC programme or the inactive control group. The TELEYOG'AVC programme will involve yoga sessions with postural, respiratory, and meditative work delivered by videoconference. This programme includes two 60-minute group sessions per week, for 12 weeks, plus one weekly home-based session (with video support). The control group will be instructed not to change their habits during the 12 weeks of experimentation, then after the final assessment (T1) they will be able to benefit from the TELEYOG'AVC programme if they want. Patients will be assessed before the experiment (T0) and after the 12-week experiment (T1). The assessments will be carried out blind, using a protocol built around the International Classification of Functioning and Disability (ICF). The main criterion is balance, assessed by the Berg balance scale (0-56 point scale). The secondary outcomes will be assessed by: Timed Up and Go Test (timed task in seconds), 5 time-sit-to-stand (timed task in seconds), the activities-specific Balance Confidence Scale - Simplified (questionnaire in %), State-Trait Anxiety Inventory (2 questionnaires out of 80), Beck Depression Inventory (score out of 63), Reintegration to Normal Living Index (score out of 22). Adherence to the programme will be assessed between T0 and T1 by the number of group and individual sessions completed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05595941
Study type Interventional
Source Hopital La Musse
Contact
Status Terminated
Phase N/A
Start date October 1, 2022
Completion date September 1, 2023

See also
  Status Clinical Trial Phase
Completed NCT04713384 - Remote Bimanual Virtual Rehabilitation Post CVD N/A
Terminated NCT04113525 - Transcutaneous Spinal and Peripheral Stimulation and Wrist Robotic Therapy for Patients With Spastic Stroke N/A
Recruiting NCT04152616 - Mechanisms of Balance Disorders in a Seated Position Following a Stroke N/A
Not yet recruiting NCT04285957 - Italian Translation and Transcultural Validation of Frenchay Activity Index and Walking Handicap Classification in Stroke
Not yet recruiting NCT05968248 - Efficacy and Safety of Deep Brain Stimulation in Mesencephalic Locomotor Region(MLR) for Poststroke Hemiplegia N/A
Recruiting NCT05964400 - duoABLE for People With Stroke and Their Caregivers N/A
Not yet recruiting NCT05210088 - PLAsticity, Security and Tolerance to Intermittent Hypoxic Conditioning Following Stroke Phase 1/Phase 2
Not yet recruiting NCT05626894 - Novel Wrist Sensor System to Promote Hemiparetic Arm Use in Home Daily Life of Chronic Stroke Survivors Phase 2
Recruiting NCT05195398 - TDCS to Improve Post-Stroke Cognitive Impairment N/A
Recruiting NCT05801874 - Gait and Posture Analysis in Hemiparetic Patients Through Optoelectronic Systems, "Smart" Tools and Clinical Evaluation
Recruiting NCT03753984 - Effects of Low-level Laser Therapy in the Fatigue Muscle of Healthy Individual and Spastic Individuals N/A
Completed NCT04116190 - A Multidisciplinary Telerehabilitation for Stroke Patients N/A
Recruiting NCT05815368 - Efficacy of REMO Training for Hand Motor Recovery After Stroke N/A
Recruiting NCT04277234 - Functional Characterisation of Post-stroke Fatigue
Not yet recruiting NCT06112574 - Cognitive-motor Training Post-stroke - a Pilot Randomized Controlled Trial N/A
Not yet recruiting NCT05595005 - Neural Bases of Post-stroke Emotion Perception Disorders
Completed NCT02644161 - Can Acupuncture Treat Post-stroke Depression? N/A
Recruiting NCT04188132 - EEG Based BCI for Upper Limb Rehabilitation in Stroke N/A
Completed NCT03651960 - Mobile and Interactive Robot's Social Acceptability for Balance and Gait Rehabilitation N/A
Active, not recruiting NCT03865173 - Post-stroke Pathway: Analysis and Link With One Year Sequelae in a French Cohort of Stroke Patients