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Contrology Training in Patients With Non-Specific Neck Pain

NCT07725978 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2026-07-24

No results posted yet for this study

Summary

This randomized controlled trial will evaluate the effects of a 12-week Contrology training program in patients with non-specific neck pain. Participants will be randomly allocated into two groups. The experimental group will receive Contrology training, while the control group will receive conventional physiotherapy. Outcomes will include pain intensity, cervical range of motion, neck-related disability, and craniovertebral angle. Assessments will be performed at baseline, 4 weeks, 8 weeks, and 12 weeks. The study aims to determine whether Contrology training is more effective than conventional physiotherapy in improving pain, posture, mobility, and functional disability in adults with non-specific neck pain.

Conditions

  • Non Specific Neck Pain

Interventions

OTHER

Contrology Training

Contrology training is a Pilates-based exercise program emphasizing concentration, control, centering, breathing, precision, and flowing movement. Participants will perform supervised exercises targeting postural correction, cervical and thoracic mobility, deep cervical flexor activation, scapular stabilization, core control, and controlled breathing for 12 weeks.

OTHER

Conventional Physiotherapy

Conventional physiotherapy will include routine exercise-based management for non-specific neck pain, including cervical range of motion exercises, stretching, strengthening exercises, postural correction, and patient education. Treatment will be provided for 12 weeks.

Sponsors & Collaborators

  • Riphah International University

    lead OTHER

Principal Investigators

  • Amna Zia · Mayo Hospital/ College of Physiotherapy, King Edward Medical University, Lahore

  • Ailia Abbas · Riphah International University, Lahore

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-30
Primary Completion
2026-09-30
Completion
2026-10-30

Countries

  • Pakistan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07725978 on ClinicalTrials.gov