Ankylosing Spondylitis Clinical Trials

Find Ankylosing Spondylitis Clinical Trials Near You

Investigation of the Effectiveness of Different Telerehabilitation Applications in Patients With Ankylosing Spondylitis

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Purpose of the study: Ankylosing spondylitis (AS) is a chronic disease that affects the spine and joints, causing pain, stiffness, fatigue, and reduced quality of life. Exercise is known to help reduce pain and improve function in individuals with AS. However, the most effective type and method of exercise are not fully known. This study aims to compare the effects of different telerehabilitation methods-synchronous (live video) and asynchronous (pre-recorded video)-on disease activity, physical function, mobility, fatigue, quality of life, kinesiophobia (fear of movement), and pain levels in individuals with AS. Study design and methods: This is a randomized controlled experimental study. Participants will be randomly assigned to one of three groups: Synchronous telerehabilitation: Exercise sessions via live video, 3 times per week for 8 weeks. Asynchronous telerehabilitation: Exercise sessions via pre-recorded videos, 3 times per week for 8 weeks. Control group: Exercise instructions provided in a brochure. All groups will perform exercises for approximately 40-50 minutes per session, focusing on flexibility, strength, posture, balance, coordination, and functional movements. Participants will be evaluated before the intervention (week 0) and after 8 weeks for disease activity, physical function, mobility, fatigue, quality of life, kinesiophobia, and pain during rest, movement, and sleep. Participants: The study will include adults aged 18-65 years diagnosed with AS at least one year prior, able to use a smartphone, and willing to participate. Individuals who are pregnant, have serious comorbidities, recent surgery, or conditions affecting mobility will be excluded. Expected benefits: The study will identify which telerehabilitation method is more effective for individuals with AS. telerehabilitation may provide easier access to treatment, improve adherence to exercise programs, and contribute to better disease management and quality of life.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 16
Maximum Age: 65
Healthy Volunteers: f
View:

• Being between the ages of 18-65

• Having been diagnosed with Ankylosing Spondylitis by a specialist at least one year ago,

• Agreeing to participate in the study voluntarily,

• Owning and being able to use a smartphone,

• Being able to read and write.

Locations
Other Locations
Turkey
Fırat University Faculty of Medicine, Department of Internal Medicine - Division of Rheumatology.
RECRUITING
Elâzığ
Time Frame
Start Date: 2025-08-01
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 66
Treatments
Experimental: Synchronous Telerehabilitation Group
Participants will receive synchronous telerehabilitation via video calls (WhatsApp) 3 times per week for 8 weeks. Each session will last 40-50 minutes and include prescribed exercise programs under live supervision.
Experimental: Asynchronous Telerehabilitation Group
Participants will receive asynchronous telerehabilitation with exercise videos delivered every 2 weeks via WhatsApp. Exercises will be performed 3 times per week for 8 weeks with feedback provided by message or phone call. An exercise diary will be used to monitor adherence.
Active_comparator: Control Group
Participants will receive a printed exercise brochure containing the same program as the intervention groups, updated every 2 weeks. They will be asked to perform the exercises 3 times per week for 8 weeks. An exercise diary will be used to monitor adherence.
Related Therapeutic Areas
Sponsors
Collaborators: Firat University
Leads: Inonu University

This content was sourced from clinicaltrials.gov