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
42 participants
INTERVENTIONAL
2025-05-01
2025-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Control Group
The treatment process for the control group consisted of hot therapy and TENS application before the exercises, followed by an exercise program including neck range of motion exercises, neck strengthening exercises, stretching exercises, scapular retraction, etc.
No interventions assigned to this group
Experimental Group
The program will be implemented over four weeks, three days a week, with a duration of 40-45 minutes per day. In addition to conventional treatment, an exercise program prepared with a light reaction time measurement and exercise set will be implemented.
Experimental Group
Participants in the experimental group will participate in a conventional exercise program similar to the control group, but with the addition of a technology-assisted exercise program. The intervention group will receive training with a reaction time measurement set using lights and an exercise set. The reaction time measurement and exercise set will be used, where light pods are placed in different positions, such as on a table, mirror, and floor, and patients will be instructed to extinguish the lit light as quickly as possible. The difficulty level of the sessions will be progressively increased by adjusting factors such as the duration of light activation, colors, the number of illuminated pods, their placement locations, and the distance between them.
Interventions
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Experimental Group
Participants in the experimental group will participate in a conventional exercise program similar to the control group, but with the addition of a technology-assisted exercise program. The intervention group will receive training with a reaction time measurement set using lights and an exercise set. The reaction time measurement and exercise set will be used, where light pods are placed in different positions, such as on a table, mirror, and floor, and patients will be instructed to extinguish the lit light as quickly as possible. The difficulty level of the sessions will be progressively increased by adjusting factors such as the duration of light activation, colors, the number of illuminated pods, their placement locations, and the distance between them.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Having neck pain persisting for at least 3 months
* Having the ability to speak and comprehend Turkish fluently
* A pain score of 3 or higher according to the Numerical Rating Scale
* A score of 5 or higher on the Neck Disability Index
Exclusion Criteria
* Having an additional musculoskeletal disorder affecting the cervical region and upper extremities (e.g., scoliosis, rheumatoid arthritis, fibromyalgia, etc.).
* Receiving physical therapy and/or other treatments for any reason within the last 6 months.
* Having a diagnosed psychiatric disorder.
* Having a vestibular pathology.
* Having visual problems despite using visual aids.
* Being pregnant.
* Having a neurological deficit that may affect balance.
* Discontinuing or being unable to complete the treatment process.
18 Years
59 Years
FEMALE
No
Sponsors
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Afyonkarahisar Health Sciences University
OTHER
Responsible Party
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Fatma Eken
Research asistant
Principal Investigators
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FATMA EKEN
Role: PRINCIPAL_INVESTIGATOR
Afyonkarahisar Sağlık Bİlimleri Üniversitesi
Locations
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Afyonkarahisar Health Sciences University
Merkez, Afyonkarahisar, 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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E-60116787-020-481633
Identifier Type: -
Identifier Source: org_study_id
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