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Clinical Trials in Turkey / NCT07489014
Enrolling by invitation Not applicable

The Effects of Mulligan Joint Mobilization and Instrument-Assisted Soft Tissue Mobilization in Individuals With Neck Pain

NCT07489014 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-13
Last updated
2026-03-23

Condition(s) studied

Neck Pain

Investigational drug(s) / intervention(s)

Instrumental Soft Tissue MobilizationMobilization

Instrumental Soft Tissue Mobilization: The treatments will administered 3 days a week for a total of 12 sessions over 4 weeks.

Mobilization: The treatments will administered 3 days a week for a total of 12 sessions over 4 weeks.

Study summary

The study will include a total of 40 individuals aged 18-65 years with chronic neck pain for at least three months. Participants will be randomly assigned to two groups: the Mulligan mobilization group (n=20) and the AYDM group (n=20). Both groups will receive a total of 12 treatment sessions, 3 days a week for 4 weeks. Assessments will be performed before and after treatment. Pain intensity will be assessed using the Visual Analog Scale (VAS), cervical awareness using the Fremantle Neck Awareness Questionnaire (FNA), and functionality using the Copenhagen Neck Functional Disability Scale (CNFDS). In addition, measurements of cervical joint range of motion, deep neck flexor muscle endurance, quality of life (SF-36), and depression level (Beck Depression Scale) will be taken.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * • Volunteering to participate in the study * Being between 18 and 65 years of age * Having experienced mechanical neck pain for at least 3 months * Not having any contraindications for manual therapy Exclusion Criteria: * Receiving a diagnosis of a psychiatric illness * Having a history of spinal surgery * Having other musculoskeletal problems that may affect the cervical region (such as scoliosis, shoulder pathologies, thoracic outlet syndrome) * Having received physiotherapy for neck and back problems within the last year.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Istanbul Rumeli University Istanbul Turkey (Türkiye)

More Istanbul Rumeli University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07489014 on ClinicalTrials.gov ↗ ← All trials in Turkey