RecruitingNot ApplicableNCT07005076

Tech-Assisted Exercise Training in Chronic Neck Pain

Investigation of the Effects of Technology-Assisted Exercises in Individuals With Chronic Neck Pain


Sponsor

Afyonkarahisar Health Sciences University

Enrollment

42 participants

Start Date

May 1, 2025

Study Type

INTERVENTIONAL

Conditions

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 chronic neck pain.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 59 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Experimental Group for people with chronic neck pain and exercise training therapy. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years to 59 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERExperimental 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.


Locations(1)

Afyonkarahisar Health Sciences University

Merkez, Afyonkarahisar, Turkey (Türkiye)

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NCT07005076


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