Tech-Assisted Exercise Training in Chronic Neck Pain
In this study, women with chronic neck pain residing in Afyonkarahisar, Turkey, will participate in an exercise-based intervention. Both the control and experimental groups will engage in conventional exercise programs; however, the experimental group will also receive an additional technology-assisted exercise program
| Condition(s) | Chronic Neck Pain, Exercise Training Therapy |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | In this study, women with chronic neck pain residing in Afyonkarahisar, Turkey, will participate in an exercise-based intervention. Both the control and experimental groups will engage in conventional exercise programs; however, the experimental group will also receive an additional technology-assisted exercise program. It is anticipated that these interventions will positively impact participants' daily living activities and functional abilities. The study aims to assess whether the inclusion of technology-supported exercises leads to superior outcomes compared to conventional exercises alone. The findings are expected to provide valuable evidence on the effectiveness of integrating technology-assisted exercise programs into physiotherapy and rehabilitation practices for women with chroni |
| Who can participate | Inclusion Criteria: * Non-specific neck pain diagnosis * 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 a history of spinal surgery. * 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 |
| Ages | 18 Years to 59 Years |
| Sex | Female |
| Lead sponsor | Afyonkarahisar Health Sciences University |
| Locations | Merkez, Afyonkarahisar, Turkey (Türkiye) |
| Start date | 2025-05-01 |
| NCT ID | NCT07005076 |
| Official listing | https://clinicaltrials.gov/study/NCT07005076 |