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NCT06295718

Tele-assessment of Functional Performance and Quality of Life in Patients With Duchenne Muscular Dystrophy: Validity and Reliability Study

Status unknown Last updated 6 March 2024
What this trial tests

trial in Duchenne Muscular Dystrophy in 20 participants. Status unknown.

Timeline
1 July 2023
Primary endpoint
2 March 2024
10 May 2024

Quick facts

Lead sponsorSahra Şirvan
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment20
Start date1 July 2023
Primary completion2 March 2024
Estimated completion10 May 2024
Sites1 location across Turkey (Türkiye)

Conditions studied

Sponsor

Sahra Şirvan

Who can join

Adults 5 to 18, male only, with Duchenne Muscular Dystrophy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Thanks to tele-assessment methods, it may be possible to evaluate DMD patients without traveling to clinical centers. In recent years, the applicability of remote assessment methods in DMD patients, as in many populations, is being investigated. However, studies have generally focused on a single evaluation parameter such as physical function, a special evaluation method or a special evaluation tool. The aim of this study is to investigate whether remote assessment of functional performance and quality of life in DMD patients is valid and reliable. If a valid and reliable tele-evaluation method that includes functional performance and quality of life parameters is found to be valid and reliable, the travel burden on patients and caregivers can be eased, patients\' stress and anxiety related to travel can be reduced, caregivers can save time and energy and provide patients with the best possible treatment.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06295718.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing