INVESTIGATION OF THE EFFECTS OF POSTURAL EXERCISES AND TAPING
OFFICE WORKERS
1 other identifier
interventional
40
1 country
1
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).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 15, 2026
CompletedStudy Start
First participant enrolled
March 15, 2026
CompletedFirst Posted
Study publicly available on registry
March 20, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 25, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2026
CompletedMarch 20, 2026
March 1, 2026
1 month
March 15, 2026
March 18, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
Depression
Beck Depression ınventory:The form contains 21 symptom categories, each with 4 options. Each item is scored between 0 and 3. The highest possible score is 63. Individuals scoring 17 points or higher are reported to have severe depressive symptoms requiring treatment.
Baseline and at the end of treatment (Week 4)
Balance test
The single-leg stance test will be used to assess balance. The individual is asked to stand on their dominant leg with their hands at their sides, then lift their leg, bending their knee joint at approximately a 45° angle, and start a stopwatch in this position. Individuals are asked to continue the test for the maximum time without losing their balance. The test ends when balance is lost, and the time is recorded in seconds.
Baseline and at the end of treatment (week 4)
Deep flexor endurance test
The 'Cervical Deep Flexor Muscle Endurance Test' is used. The test was performed in a supine hook position. The participants' hands were placed loosely on their abdomen. The person was instructed to pull their chin inward (chin tuck) and, while maintaining this position, to lift their head off the bed.
Baseline and at the end of treatment (week 4)
SF 36 Quality of life
The Short Form-36 (SF-36) is a scale consisting of 36 questions that assess a person's health status with 8 sub-items (physical function (FF), physical health (FS), emotional problems (DS), energy fatigue (EF), emotional state (DD), social function (SF), pain (A), general health (GS)). Each sub-item is scored separately on a scale of 0-100. The closer the score is to 100, the better the health status.
Baseline and at the end of treatment (week 4)
Pain Assessment
Visual pain Assessment is used. Individuals were asked to indicate the intensity of the pain they felt on a 10 cm long scale (0: no pain, 10: unbearable pain).
Baseline and at the end of treatment (week 4)
Disability
Neck disability index is used.The questionnaire, which assesses subjective symptoms and daily living activities, consists of 10 sections in total (pain intensity, personal care, lifting, reading, headache, concentration, work life, driving, sleep, and leisure activities). Each section has 6 items ranging from 0 to 5 points. The total score ranges from 0 to 50 (0: no disability; 50: maximum disability).
Baseline and at the end of treatment (week 4)
Study Arms (3)
kinesiotape group
EXPERIMENTALParticipants in this group undergo Kinesio Taping treatment to correct kyphosis.
exercise group
ACTIVE COMPARATORneck and posture exercises were given to the participants.
Control
NO INTERVENTIONControl group didnt attend any program or intervention
Interventions
Neck and posture exercises will be given to the participants Third times a week for four weeks.
Eligibility Criteria
You may qualify if:
- Those who have had neck pain for at least 3 months, Those who have worked at a desk for at least 3 years, Those who work at a computer for at least 6 hours or more a day during working hours, Those who sign the voluntary consent form.
You may not qualify if:
- Individuals who have received any physiotherapy program due to neck or back pain within the last 3 months, those with acute torticollis, those who have undergone cervical spine surgery, those with a history of fractures in the cervical vertebrae, those with conditions that will prevent evaluation or communication (such as cognitive problems), individuals with proven specific pathological conditions such as malignancy, fracture, systemic rheumatoid disease, or other musculoskeletal problems that may also affect the cervical region, such as impingement and thoracic outlet, those allergic to kinesiobands
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul Rumeli University
Istanbul, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
March 15, 2026
First Posted
March 20, 2026
Study Start
March 15, 2026
Primary Completion
April 25, 2026
Study Completion
April 30, 2026
Last Updated
March 20, 2026
Record last verified: 2026-03