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

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

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07489014
Enrollment
40
Registered
2026-03-23
Start date
2026-03-13
Completion date
2026-04-30
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain

Keywords

neck pain, mulligan, instrument-assisted soft tissue mobilization, cervical awareness, function, pain

Brief 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.

Interventions

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

OTHERMobilization

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

Sponsors

Istanbul Rumeli University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 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.

Design outcomes

Primary

MeasureTime frameDescription
Pain IntensityBaseline and at the end of treatment (week 4)Visual Pain Scale.Participants' pain intensity will be assessed using the Visual Analog Scale (VAS). The Visual Analog Scale is a validated and reliable scale that quantitatively determines the intensity of pain perceived by an individual. The scale consists of a 10 cm long horizontal or vertical line, with one end of the line defined as "0 = no pain" and the other end as "10 = unbearable pain".
Range of motionBaseline and at the end of treatment (week 4)To assess the active range of motion of the cervical joint, the tape measure method described by Hsieh et al. (1986) was used. This method is reported to be a practical and reliable measurement tool for assessing cervical range of motion in clinical practice.
Cervical awarenessBaseline and at the end of treatment (week 4)Fremantle Neck Awareness Questionnaire
Copenhagen Neck Functional Disability ScaleBaseline and at the end of treatment (week 4)Neck Functional Disability is a 15-item questionnaire. Total score(0-30) indicate higher disability

Secondary

MeasureTime frameDescription
Neck flexor enduranceBaseline and at the end of treatment (week 4)The test protocol is performed with the individual in a supine position, with knees bent and soles of feet touching the ground (hook position). Individuals are asked to comfortably position their hands on their abdominal area. During the procedure, the physiotherapist places their index and middle fingers overlapping under the participant's head. Participants are first instructed to pull their chin inward and downward (chin-tuck) and, while maintaining this position, to perform active craniocervical flexion, raising their head approximately 2.5 cm above the physiotherapist's fingers. The maximum time participants canmaintain this position without breaking it was recorded in seconds using a stopwatch.
SF-36 Quality of lifeBaseline and at the end of treatment (week 4)The SF-36 does not have a total scoring system; assessment is based on eight sub-dimensions: physical function, physical role difficulty, emotional role difficulty, social function, mental health, energy (vitality), pain, and general health perception.
Depression ScaleBaseline and at the end of treatment (week 4)Beck Depression Scale is a psychological status-based scale consisting of 21 items developed to assess an individual's recent emotional state. Each item on the scale is scored between 0 and 3, and the level of depression is determined based on the total score obtained.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026