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Ankylosing SpondylitisNCT06392620

Telerehabilitation in Ankylosing Spondylitis

A study testing Study Group in people with Ankylosing Spondylitis, run by Firat University at 1 site in Turkey (Türkiye).

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Ankylosing Spondylitis (AS) is an inflammatory rheumatic disease primarily affecting the spine and sacroiliac joint. xercise is one of the most important nonpharmacologic treatment modalities in AS. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Ankylosing Spondylitis
What is being tested?
Study Group
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteTurkey (Türkiye)
Study dates
20 Apr 2024to 20 Jul 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 18-65 years old
  • Patients whose medical treatment has not changed in the last three months
  • Patients with a diagnosis of AS will be included.

Who cannot join

  • Patients who are pregnant
  • Patients with a diagnosis of malignancy
  • Patients with other concomitant systemic inflammatory rheumatic diseases
  • Patients with neurological, orthopedic or congenital problems that prevent physical activity
  • Patients with regular exercise habits will be excluded from the study

Trial locations and contacts

1 site in 1 country.

Songul Baglan Yentur contact

+90 424 2370000

songulbaglan23@hotmail.com

Turkey (Türkiye)1 site, 1 recruiting
  • Songul Baglan Yentur

    Elâzığ, Elâzığ, 23100

    Songul Baglan Yentur, 04242370000, songulbaglan23@hotmail.com

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Official title: Effects of Telerehabilitation in Patients With Ankylosing Spondylitis

Ankylosing Spondylitis (AS) is an inflammatory rheumatic disease primarily affecting the spine and sacroiliac joint. xercise is one of the most important nonpharmacologic treatment modalities in AS. Stretching, strengthening, aerobic, posture, balance and moltimodal exercise methods are the most commonly used treatment methods. The study will include 44 patients diagnosed with AS aged 18-65 years. Patients will be divided into two randomized controlled groups with 22 patients in each group. Group 1 will receive a personalized exercise program including stretching, strengthening, respiratory, aerobic and posture exercises via video conferencing. Group 2 will be recommended a video on the YouTube platform and will be asked to perform the exercises by following the content of these videos. Spinal mobility will be assessed with Bath Ankylosing Spondylitis Metrology Index, disease activity with Bath Ankylosing Spondylitis Disease Activity Index, function with Bath Ankylosing Spondylitis Function Index, quality of life with Ankylosing Spondylitis Quality of Life Scale and posture with PostureScreeen mobile application.

Read the detailed description

Ankylosing Spondylitis (AS) is an inflammatory rheumatic disease primarily affecting the spine and sacroiliac joint. It usually begins in the second decade of life and is more common in men than women. The benefits of exercise and physical activity in health and disease are well recognized. Exercise is one of the most important nonpharmacologic treatment modalities in AS. Stretching, strengthening, aerobic, posture, balance and moltimodal exercise methods are the most commonly used treatment modalities. However, the application of these exercise methods to patients with AS in the form of a home exercise program is advantageous due to its low cost and the ease with which patients can start exercising. The study will include 44 patients diagnosed with AS aged 18-65 years. Patients will be divided into two randomized controlled groups with 22 patients in each group. Group 1 will receive a personalized exercise program including stretching, strengthening, respiratory, aerobic and posture exercises via video conferencing. Group 2 will be recommended a video on the YouTube platform and will be asked to perform the exercises by following the content of these videos. Patients in Group 2 will be followed up by regular communication with the patients and by asking the patient to create an attendance chart. Patients in both groups will receive the treatment 3 days a week for 8 weeks. Evaluation methods will be applied at the beginning and at the end of the treatment. Spinal mobility will be assessed with Bath Ankylosing Spondylitis Metrology Index, disease activity with Bath Ankylosing Spondylitis Disease Activity Index, function with Bath Ankylosing Spondylitis Function Index, quality of life with Ankylosing Spondylitis Quality of Life Scale and posture with PostureScreeen mobile application.

Being tested
Study Group
Keywords
Ankylosing Spondilitis,, Exercise, YouTube
Medical subject headings
Spondylitis, Ankylosing, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Study GroupOther

    n individually planned exercise program including stretching, strengthening, respiratory, aerobic and posture exercises will be applied via video conference method

Study groups in NCT06392620
Study groupRoleWhat they receive
Study groupExperimentalAn individually planned exercise program including stretching, strengthening, respiratory, aerobic and posture exercises will be applied via video conference method.
Receives: Other: Study Group
Control groupExperimentalIt will be recommended a video on YouTube platform and will be asked to do the exercises by following the content of these videos
Receives: Other: Study Group

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Spinal mobility

    Spinal mobility will be assessed and scored with BASMI. According to the index, there are five measurements: lateral lumbar flexion, tragus-wall distance, lumbar flexion (Modified Schober), maximal intermalleolar distance and cervical rotation.

    Measured: 10 minutes

Secondary outcomes (2)
  1. Disease activity

    Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) consisting of 6 questions will be used to assess disease activity.

    Measured: 1 minute

  2. Function

    BASFI will be used to assess function. The index includes 10 questions about activities of daily living. A 10 cm VAS will be used for each question

    Measured: 2 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Apr 2024
  2. Study start20 Apr 2024 (estimated)
  3. Primary completion20 Jun 2024 (estimated)
  4. Study completion20 Jul 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06392620
Sponsor's protocol ID
2024/03-08
Status last verified
Apr 2024
First submitted
26 Apr 2024
Last updated
30 Apr 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Yentur SB, Boyrazli IS, Elbasti MS, Koca SS. Effects of telerehabilitation and YouTube platform-based exercise videos in patients with axial spondyloarthritis: a randomized controlled study. Clin Rheumatol. 2025 Sep;44(9):3561-3571. doi: 10.1007/s10067-025-07591-w. Epub 2025 Jul 25.

    PubMed 40715923

Questions about this trial

What is this clinical trial studying?

A study testing Study Group in people with Ankylosing Spondylitis, run by Firat University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 30 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Songul Baglan Yentur (+90 424 2370000, songulbaglan23@hotmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Spinal mobility (time frame: 10 minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06392620, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Apr 2024.

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