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Recruiting NCT07605013

NCT07605013 Mobilization Techniques for Nonspecific Neck Pain: Effects on Cervical Endurance and Function

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Clinical Trial Summary
NCT ID NCT07605013
Status Recruiting
Phase
Sponsor Istanbul University - Cerrahpasa
Condition Neck Pain Musculoskeletal
Study Type INTERVENTIONAL
Enrollment 51 participants
Start Date 2026-03-16
Primary Completion 2027-01-16

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 40 Years
Study Type INTERVENTIONAL
Interventions
Positional Release Technique (PRT)Instrument-Assisted Soft Tissue Mobilization (İASTM)Control Group

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 51 participants in total. It began in 2026-03-16 with a primary completion date of 2027-01-16.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This clinical study investigates the comparative effects of two manual therapy mobilization techniques, Positional Release Technique (PRT) and Instrument-Assisted Soft Tissue Mobilization (İASTM), on cervical muscle endurance and functional performance in individuals with nonspecific neck pain. Nonspecific neck pain is a common musculoskeletal condition among office workers and students, often associated with poor posture, prolonged sitting, and repetitive strain. It leads to reduced muscle endurance, impaired functional capacity, and decreased quality of life. Early and effective management strategies are essential to prevent chronicity and disability. A total of 51 participants will be recruited and randomly assigned into three groups: Group 1 will receive PRT combined with a standardized home exercise program, Group 2 will receive İASTM combined with the same home exercise program, and Group 3 will serve as the control group receiving only conventional home exercise. The interventions will be delivered over a period of 4 weeks, with three sessions per week, under the supervision of trained physiotherapists. The home exercise program includes stretching, strengthening, and posture correction exercises designed to support cervical spine health. The primary outcomes of the study are cervical muscle endurance and functional performance, measured using validated clinical tests. Secondary outcomes include pain intensity assessed by the Visual Analog Scale (VAS), functional disability measured by the Neck Disability Index (NDI), health-related quality of life assessed by the SF-12 questionnaire, and work-related performance indicators. Assessments will be conducted at baseline and after 4 weeks of intervention. Randomization and blinding procedures will be applied to minimize bias, and standardized protocols will ensure consistency across groups. The main objective of this study is to determine whether the early application of PRT or İASTM, in combination with home exercise, provides superior improvements in cervical muscle endurance, pain reduction, and functional outcomes compared to exercise alone. By comparing these two mobilization techniques, the study aims to contribute evidence-based knowledge to physiotherapy practice and guide clinicians in selecting effective manual therapy approaches for nonspecific neck pain. The findings are expected to support clinical decision-making, improve patient care, and enhance rehabilitation strategies for individuals suffering from neck pain in occupational and daily life contexts.

Eligibility Criteria

Inclusion Criteria: * Healthy individuals aged 18-40 years * Individuals working at a desk job (office or remote) for at least 6 hours per day * Physically active individuals with no neck pain (NPRS score 0-2) * Voluntary consent to participate in the study Exclusion Criteria: * History of neck trauma, surgery, or any cardiovascular, metabolic, neurological, or rheumatoid arthritis condition within the last 6 months * Participation in a manual therapy or physiotherapy program within the last 6 months * Presence of severe malignancy, rheumatoid arthritis, or cardiovascular disease * Pregnancy or breastfeeding

Contact & Investigator

Central Contact

GUNEY SHIRVANOVA, BSc PT

✉ guneyshirvanova@ogr.iuc.edu.tr

📞 +994515765931

Principal Investigator

GUNEY SHIRVANOVA, BSc PT

PRINCIPAL INVESTIGATOR

Istanbul University-Cerrahpasa, Department of Physical Therapy and Rehabilitation

Frequently Asked Questions

Who can join the NCT07605013 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 40 Years, studying Neck Pain Musculoskeletal. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07605013 currently recruiting?

Yes, NCT07605013 is actively recruiting participants. Contact the research team at guneyshirvanova@ogr.iuc.edu.tr for enrollment information.

Where is the NCT07605013 trial being conducted?

This trial is being conducted at Istanbul, Turkey (Türkiye).

Who is sponsoring the NCT07605013 clinical trial?

NCT07605013 is sponsored by Istanbul University - Cerrahpasa. The principal investigator is GUNEY SHIRVANOVA, BSc PT at Istanbul University-Cerrahpasa, Department of Physical Therapy and Rehabilitation. The trial plans to enroll 51 participants.

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