Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2026-03-26 @ 3:16 PM
Ignite Modification Date:
2026-03-26 @ 3:16 PM
NCT ID:
NCT07486232
Brief Summary:
The aim of this randomized controlled trial is to evaluate and compare the efficacy of Kinesio Taping (KT) and a structured exercise program on pain, disability, balance, and psychosocial well-being in desk-based office workers with chronic neck pain.
Background:
Prolonged sedentary work, particularly desk jobs exceeding six hours per day, is a significant risk factor for chronic neck pain and postural dysfunction. This study focuses on employees of the Kocaeli Governorate to determine which conservative intervention-active (exercise) or passive/supportive (taping)-provides superior clinical outcomes.
Methods:
A total of 45 volunteers (minimum 15 per group) aged 25-55, who work at desks for at least six hours a day and suffer from chronic neck pain, will be enrolled. Participants will be randomly assigned to one of three groups for a 4-week intervention period:
Kinesio Taping Group: Participants will receive therapeutic taping for the cervical region.
Exercise Group: Participants will undergo a structured program focusing on neck stabilization and postural correction.
Control Group: Participants will receive no active intervention and will maintain their routine activities.
Outcome Measures:
Comprehensive assessments will be conducted at baseline and at the end of the 4-week program:
Pain \& Disability: Visual Analog Scale (VAS) and Neck Disability Index (NDI).
Physical Performance: Balance tests and Deep Neck Flexor Endurance test.
Psychosocial Status: Quality of Life (SF-36) and depression levels (Beck Depression Inventory).
Study:
NCT07486232
Study Brief:
Protocol Section:
NCT07486232