NCT07751601

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Nov 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 22, 2026

Completed
27 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 18, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

July 26, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

August 7, 2026

Completed
Last Updated

August 7, 2026

Status Verified

August 1, 2026

Enrollment Period

6 months

First QC Date

July 26, 2026

Last Update Submit

August 5, 2026

Conditions

Keywords

Non-Specific Neck Straincervical exercisemanipulationboyun ağrısıcervical region

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 COMPARATOR

Participants 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.

Other: Manipulation and Exercise

Mobilization and Exercise Group

ACTIVE COMPARATOR

Participants 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.

Other: Mobilization and Exercise

Exercise Only Group

ACTIVE COMPARATOR

Participants 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.

Behavioral: Standardized Exercise Program

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.

Manipulation and Exercise Group

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).

Mobilization and Exercise Group

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.

Exercise Only Group

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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)

Location

MeSH Terms

Interventions

Exercise

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Gamze BAŞKENT, Dr

    Istanbul Rumeli University

    STUDY DIRECTOR

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
Model Details: This is a parallel-group study with three arms. Participants are randomly assigned to one of the following groups: Group 1 receives manipulation and exercise; Group 2 receives mobilization and exercise; and Group 3 (control group) receives only exercise.
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.

Locations