Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
160 participants
INTERVENTIONAL
2025-09-30
2026-03-26
Brief Summary
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Detailed Description
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Material-Method:
In this study, it was planned to investigate the effects of stretching and sacroiliac mobilization exercises on musculoskeletal pain and sacroileitis, which are side effects of the drug, on musculoskeletal pain and quality of life in patients started on isotretinoin treatment. Between August 2025 and January 2026, patients who applied to the dermatology outpatient clinic and planned to start isotretinoin will be informed about the study, one group will be taught a sacroiliac stretching and mobilization exercise program and will be asked to perform these exercises 10 times in 2 sets every day. The other group will consist of patients who do not exercise and take medication. Within the scope of this prospectively planned study, it is planned to evaluate the patients by collecting data in 4 stages. The first stage will be collected before the start of isotretinoin treatment, the second stage in the 1st month of treatment, the third stage in the 3rd month of treatment and the last stage in the 6th month of treatment by evaluating pain measurement and quality of life. Musculoskeletal pain measurements, quality of life, and conditions occurring during follow-up will be evaluated and compared between the exercising group and the non-exercising group.
Pain measurement; The pain sensitivity of the subjects to pressure will be evaluated with a pain meter device called algometer. Algometer Commender Jtech Medical 801-478 USA brand digital algometer will be used in the evaluation. This device is already in current use and belongs to the researchers themselves. The algometer will be used to measure the trapezius muscle trunk, latissimus dorsi muscle trunk and sacroiliac joints bilaterally 3 times each. Before the measurement, the areas will be marked and the algometer will be placed perpendicular to these points and the subjects will be asked to report the first sensation of pain. The pain threshold will be recorded in pounds (1kg=2.2 pounds) by reading the value on the indicator.
Quality of Life measurement; World Health Organization Quality of Life (WHOQOL-SHORT FORM) is a statement-based measure developed to assess perception, personal goals, standards and concerns within one's own culture and values. The WHOQOL-SHORT FORM measures the following domains: physical health, psychological health, social relationships and environment. High scores indicate high quality of life, while low scores indicate low quality of life. Turkish validity and reliability has been realized (4).
Hypothesis(es): Regular exercises will have a positive effect on pain and quality of daily life levels in patients started on isotretinoin treatment.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Sacroiliac (SI) joint exercise group
This 18-week, 5-day-a-week program is a comprehensive plan designed to build stability, strength, and mobility progressively while being mindful of the sensitivity of the SI joint.
This program is divided into three 6-week phases. Each week consists of 5 sessions, mixing different focuses to ensure balanced development.
Day 1: Foundational Strength \& Stability
Day 2: Low-Impact Cardio \& Active Recovery
Day 3: Core Focus \& Hip Stability
Day 4: Low-Impact Cardio \& Mobility
Day 5: Full Body Integration \& Strength
Exercise
The 18-Week Program Structure This program is divided into three 6-week phases. Each week consists of 5 sessions, mixing different focuses to ensure balanced development.
Day 1: Foundational Strength \& Stability
Day 2: Low-Impact Cardio \& Active Recovery
Day 3: Core Focus \& Hip Stability
Day 4: Low-Impact Cardio \& Mobility
Day 5: Full Body Integration \& Strength
Control group
Control group: No intervention
No interventions assigned to this group
Interventions
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Exercise
The 18-Week Program Structure This program is divided into three 6-week phases. Each week consists of 5 sessions, mixing different focuses to ensure balanced development.
Day 1: Foundational Strength \& Stability
Day 2: Low-Impact Cardio \& Active Recovery
Day 3: Core Focus \& Hip Stability
Day 4: Low-Impact Cardio \& Mobility
Day 5: Full Body Integration \& Strength
Eligibility Criteria
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Inclusion Criteria
* Not having a regular exercise habit,
* Starting Isotretinoin treatment for the first time.
Exclusion Criteria
* The presence of any diagnosed neurological disease,
* Having any diagnosed psychiatric illness,
* Having a physical disability that prevents them from exercising for any reason.
18 Years
35 Years
ALL
No
Sponsors
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Uşak University
OTHER
Responsible Party
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Asli keles onal
MD
Principal Investigators
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Ali Y Karahan, MD
Role: STUDY_DIRECTOR
Uşak University
Locations
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Usak University
Uşak, , Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Asli1
Identifier Type: -
Identifier Source: org_study_id
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