Comparison of Manipulation, Mobilization, and Exercise for Nonspecific Neck Tension
Evaluation of the Effects of Manipulation, Mobilization, and Neck Exercises in Individuals With Nonspecific Neck Tension
1 other identifier
interventional
60
1 country
1
Brief Summary
The primary purpose of this study is to investigate and compare the effects of different physiotherapy approaches, such as manipulation, mobilization, and neck exercises, on pain, range of motion, neck functionality, quality of life, muscle tightness, and psychological status in individuals with non-specific neck tension. Throughout the study, the clinical, physical, and myofascial parameters, as well as the psychological statuses of the patients, were recorded through detailed evaluations conducted before and after the treatment, within the framework of a treatment program planned as 2 sessions per week for a total of 8 sessions over 4 weeks.
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 Nov 2025
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
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 22, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 18, 2026
CompletedFirst Submitted
Initial submission to the registry
July 26, 2026
CompletedFirst Posted
Study publicly available on registry
August 7, 2026
CompletedAugust 7, 2026
August 1, 2026
6 months
July 26, 2026
August 5, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Visual Analog Scale
Measurement of pain intensity.
At baseline and the 4-week treatment period.
Secondary Outcomes (1)
Goniometric Measurement (ROM)
At baseline and the 4-week treatment period.
Other Outcomes (4)
Copenhagen Neck Functional Disability Scale
At baseline and the 4-week treatment period.
Short Form-36 (SF-36)
At baseline and the 4-week treatment period.
Hospital Anxiety and Depression Scale - Anxiety Subscale
At baseline and the 4-week treatment period.
- +1 more other outcomes
Study Arms (3)
Manipulation and Exercise Group
ACTIVE COMPARATORParticipants in this group receive a comprehensive intervention consisting of cervical manipulation (general cervical, C1), and thoracic manipulation, combined with a standardized exercise program. The exercise program includes neck flexion, extension, lateral flexion, rotation, pectoral and trapezius stretching, and chin tuck exercises.
Mobilization and Exercise Group
ACTIVE COMPARATORParticipants in this group receive a comprehensive intervention consisting of cervical mobilization (C2-C4 levels), thoracic mobilization, traction with rotation, and anterior-posterior/lateral gliding techniques, combined with the same standardized exercise program as the other groups. The exercise program includes neck flexion, extension, lateral flexion, rotation, pectoral and trapezius stretching, and chin tuck exercises.
Exercise Only Group
ACTIVE COMPARATORParticipants in this group receive only the standardized exercise program. This program includes neck flexion, extension, lateral flexion, rotation, pectoral and trapezius stretching, and chin tuck exercises.
Interventions
Participants undergo cervical (general, C1) and thoracic manipulation, followed by a standardized exercise program including neck range of motion exercises (flexion, extension, lateral flexion, rotation), pectoral and trapezius stretching, and chin tucks.
Participants undergo cervical (C2-C4) and thoracic mobilization, traction with rotation, and gliding techniques (anterior-posterior/lateral), followed by the same standardized exercise program as mentioned above (neck ROM, stretching, chin tucks).
Participants perform only the standardized exercise program consisting of neck range of motion exercises (flexion, extension, lateral flexion, rotation), pectoral and trapezius stretching, and chin tuck exercises.
Eligibility Criteria
You may qualify if:
- \- Non-specific neck muscle tension
- Being between 18-30 years of age
- Not having a chronic disease
- Not having undergone any surgery,
- Having limited mobility in the cervical region
- Having at least 2 pains according to the Visual Analog Scale at rest
- Individuals with subacute and chronic non-specific neck pain were included in this study
- Having a negative vertebrobasilar artery test
You may not qualify if:
- Having a chronic systemic disease
- Having cervical straightening and cervical herniation (with a diagnosis and report)
- Having undergone surgery
- Having instability in the cervical joints and trauma within the last year
- Having severe osteoporosis
- Having neurological findings
- Having received physical therapy within the last 6 months
- Having vertigo
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
İstanbul Rumeli Üniversitesi
Istanbul, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Gamze BAŞKENT, Dr
Istanbul Rumeli University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- The outcome assessor was blinded to group allocation. However, the physical therapist (care provider) and the participants were not blinded due to the nature of the physical therapy interventions.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Physiotherapist
Study Record Dates
First Submitted
July 26, 2026
First Posted
August 7, 2026
Study Start
November 25, 2025
Primary Completion
May 22, 2026
Study Completion
June 18, 2026
Last Updated
August 7, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share
Individual participant data (IPD) are not shared publicly in order to protect participant confidentiality and comply with the data retention policies specified in the ethics committee approval form.