TeleRehabilitation for Patients With Chronic Respiratory Failure.

NCT04566523 | Unknown DMC

• 1 other identifier: 2019-102868-49
• Study Type: observational
• Target: 220
• Locations: 1 country
• Sites: 1

Brief Summary

It is widely described in the literature that exercise training improves patients' exercise tolerance, quality of life, symptoms, anxiety and depression, regardless of the location. Despite overwhelming evidence of the benefits of exercise training, only a very small percentage of eligible people have ever completed a program. Alternative modes of exercise training are needed to improve equity of access for patients with chronic respiratory disease. So TeleRehabilitation, using information and communication technologies to provide distance exercise training services, may be an answer.

Conditions

Chronic Respiratory Disease; Exercise

Outcome Measures

Primary Outcomes (1)

• exercise tolerance

  number of steps during 6 minute stepper test

  3 month after inclusion

Secondary Outcomes (3)

• exercise tolerance

  6 month and one year after inclusion

• VQ-11

  3, 6 month and 1 year after inclusion

• physical activity quantity

  3, 6 month and 1 year after inclusion

Study Arms (2)

Control Group

Chronic respiratory patients who undergo a home-based exercise training program with a rehabilitation coach supervision.

Tele Group

Chronic respiratory patients who undergo a home-based exercise training program online.

Other: telerehabilitation

Interventions

telerehabilitation OTHER

Patients undergo an online exercise training program via a certified host of health data website.

Tele Group

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

patients from medical consultation

You may qualify if:

• chronic respiratory disease patients
• Patients with dyspnea or exercise intolerance.
• Stable patients at home.
• Patients who can use a computer (after explanations) and have adequate hearing and vision.
• Collection of the patient's non-objection

You may not qualify if:

• Life expectancy \<3 months.
• Absolute contraindication to performing physical activity

Sponsors & Collaborators

• SOS Oxygene Mediterranee: lead

Study Sites (1)

Cabinet de pneumologie Clinique des Cèdres

Cornebarrieu, 31700, France

RECRUITING

MeSH Terms

Conditions

Motor Activity

Interventions

Telerehabilitation

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Rehabilitation; Aftercare; Continuity of Patient Care; Patient Care; Therapeutics; Health Services; Health Care Facilities Workforce and Services; Telemedicine; Delivery of Health Care; Patient Care Management; Health Services Administration

Study Officials

• william Heurtaux, MD

  Clinique des Cèdres

  PRINCIPAL INVESTIGATOR

Central Study Contacts

delphine delample, PhD

CONTACT

+33612155648; d.delample@sosoxygene.com

Study Design

• Study Type: observational
• Observational Model: CASE CONTROL
• Time Perspective: PROSPECTIVE
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 22, 2020
• First Posted: September 28, 2020
• Study Start: September 1, 2020
• Primary Completion: September 1, 2025
• Study Completion: September 1, 2025
• Last Updated: November 28, 2023

Record last verified: 2023-11

Data Sharing

• IPD Sharing: Will not share

Locations

FR (1)