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NCT04683809 Clinical Trial

Effects of a Telerehabilitation Approach in Children With Cystic Fibrosis

Cystic Fibrosis Clinical Trial

Official title:
The Effect of Telerehabilitation on Quality of Life, Anxiety and Depression Levels in Children With Cystic Fibrosis and Their Caregivers

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04683809
Other study ID # 1442
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 2021
Est. completion date June 2021

Study information
Verified date December 2020
Source Marmara University
Contact Ozge Kenis-Coskun
Email ozgekenis@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients with cystic fibrosis aged 6-13 will be recruited and randomized into two groups: one will receive telerehabilitation sessions including postural, breathing and high-intensity interval training exercises and one will be subject to routine follow up. Exercise program will be applied three days a week for three months. Children will be assessed by pulmonary function tests, cystic fibrosis quality of life questionnaire, six minute walking test and anxiety and depression scale in children, while caregivers will be assessed by Beck depression scale and situational anxiety inventory.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 30
Est. completion date June 2021
Est. primary completion date May 2021
Accepts healthy volunteers No
Gender All
Age group 6 Years to 13 Years
Eligibility Inclusion Criteria: - Patients with diagnosed cystic fibrosis Exclusion Criteria: - Current pulmonary exacerbation - Musculoskeletal problems hinder exercising - No internet access - Patients and parents do not consent to intervention

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Telerehabilitation
Patients will attend rehabilitation sessions through online programmes for rehabilitation

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Marmara University

Outcome
Type Measure Description Time frame Safety issue
Primary Cystic fibrosis quality of life questtionaire Cystic fibrosis quality of life questtionaire 3 months
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