Viewing Study NCT07486232


Ignite Creation Date: 2026-03-26 @ 3:16 PM
Ignite Modification Date: 2026-03-31 @ 1:51 AM
Study NCT ID: NCT07486232
Status: ENROLLING_BY_INVITATION
Last Update Posted: 2026-03-20
First Post: 2026-03-15
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: INVESTIGATION OF THE EFFECTS OF POSTURAL EXERCISES AND TAPING
Sponsor: Istanbul Rumeli University
Organization:

Study Overview

Official Title: INVESTIGATION OF THE EFFECTS OF POSTURAL EXERCISES AND TAPING IN OFFICE WORKERS WITH CHRONIC NECK PAIN
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2026-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: OFFICE WORKERS
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).
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: