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ENROLLING BY INVITATION
NCT07489014
NA

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

Sponsor: Istanbul Rumeli University

View on ClinicalTrials.gov

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.

Official title: Comparison of the Effects of Mulligan Joint Mobilization and Instrument-Assisted Soft Tissue Mobilization on Pain Intensity, Cervical Awareness, and Functionality in Individuals With Chronic Neck Pain

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2026-03-13

Completion Date

2026-04-30

Last Updated

2026-03-23

Healthy Volunteers

No

Conditions

Interventions

OTHER

Instrumental Soft Tissue Mobilization

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

OTHER

Mobilization

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

Locations (1)

Istanbul Rumeli University

Istanbul, Turkey (Türkiye)