Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07150143

Effects of Connective Tissue Massage and Physical Modalities Combined With Stabilization Exercises in Chronic Neck Pain

Comparative Effects of Connective Tissue Massage and Physical Modalities Added to Cervical and Scapulothoracic Stabilization Exercises on Pain, Function, and Endurance in Individuals With Chronic Neck Pain

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
27 (estimated)
Sponsor
Fenerbahce University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This randomized, double-blinded controlled trial aims to investigate the comparative effects of connective tissue massage and physical modalities, when combined with cervical and scapulothoracic stabilization exercises, in individuals with chronic non-specific neck pain. A total of 51 participants aged 18-65 years will be randomly assigned into three groups. Group 1 will perform stabilization exercises alone, Group 2 will receive stabilization exercises plus connective tissue massage, and Group 3 will receive stabilization exercises plus electrotherapy modalities (infrared, continuous ultrasound, and TENS). The interventions will be conducted twice weekly for 8 weeks, and participants will also perform home-based exercises daily. Primary outcomes include pain, disability, and endurance, while secondary outcomes focus on quality of life, cervical range of motion, and scapular function.

Detailed description

Chronic non-specific neck pain is a prevalent musculoskeletal disorder that adversely affects pain, functional capacity, and quality of life. Stabilization-based exercise programs are commonly recommended; however, the added benefits of connective tissue massage and physical modalities require further investigation. This randomized, double-blinded controlled trial is designed to compare the effects of (1) stabilization exercises alone, (2) stabilization exercises combined with connective tissue massage, and (3) stabilization exercises combined with electrotherapy modalities (infrared therapy, continuous ultrasound, and TENS) on clinical outcomes in individuals with chronic non-specific neck pain. A total of 51 participants between 18 and 65 years of age will be randomly allocated into three equal groups. All groups will receive supervised exercise sessions twice weekly for 8 weeks, each lasting 50 minutes (10 minutes of warm-up, 30 minutes of cervical and scapulothoracic stabilization, and 10 minutes of cool-down). Additionally, participants will be instructed to perform a one-hour home exercise program daily, supported with illustrated brochures. The primary outcomes are: * Pain (Bournemouth Neck Questionnaire) * Disability (Neck Disability Index) * Endurance (Deep Cervical Flexor Test) The secondary outcomes are: * Quality of life (WHOQOL-BREF) * Cervical range of motion * Scapular function (Lateral Scapular Slide Test and Scapular Dyskinesis Test) By comparing these approaches, the study aims to determine whether the addition of connective tissue massage or physical modalities enhances the therapeutic effects of stabilization exercises on pain, function, and endurance in patients with chronic non-specific neck pain.

Conditions

Interventions

TypeNameDescription
OTHERExerciseEach exercise session lasts 50 minutes, consisting of a 10-minute warm-up, 30 minutes of stabilization exercises, and a 10-minute cool-down. Stabilization exercises are selected from an exercise pool according to the individual's needs, with progression ensuring throughout the program. The exercises will be administered face-to-face twice a week for eight weeks, and participants will be provided with illustrated brochures and instructed to perform a one-hour home exercise program daily.
OTHERConnective tissue massageConnective tissue massage will be applied, starting from the basic regions and gradually incorporating other regions.
OTHERInfrared therapyInfrared therapy will be applied for 20 minutes
OTHERContinuous ultrasoundContinuous ultrasound will be applied to the right and left sides for 7 minutes each at an intensity of 2 W/cm².
OTHERConventional TENS20 minutes of conventional TENS will be administered to the painful area.

Timeline

Start date
2025-09-12
Primary completion
2025-11-01
Completion
2026-10-01
First posted
2025-09-02
Last updated
2025-09-18

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07150143. Inclusion in this directory is not an endorsement.