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

F

Fenerbahce University

Status

Enrolling

Conditions

Non-specific Neck Pain

Treatments

Other: Connective tissue massage
Other: Continuous ultrasound
Other: Conventional TENS
Other: Infrared therapy
Other: Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT07150143
2015-KAEK-63-22-07

Details and patient eligibility

About

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.

Full 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.

Enrollment

27 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being between 18 and 65 years of age,
  • Having non-specific chronic neck pain localized to the posterior cervical spine between the occipital region and the spinous process of the first thoracic vertebra,
  • Being able to cooperate with the assessments to be performed in the study.

Exclusion criteria

  • Neck pain resulting from trauma within the past 6 months;
  • A history of surgery related to cervical problems;
  • Clinical signs of cervical radiculopathy and/or myelopathy;
  • Inflammatory arthritis involving the cervical spine;
  • Tumors or infections of the cervical spine;
  • Vertebrobasilar artery insufficiency;
  • Neurological disorders (such as multiple sclerosis, Parkinson's disease, or syringomyelia);
  • Congenital anomalies affecting the spine; systemic diseases (such as diabetes mellitus);
  • Shoulder pathologies (including tendinitis, bursitis, or capsulitis).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

27 participants in 3 patient groups

Exercise
Active Comparator group
Description:
Each exercise session lasts 50 minutes, consisting of 10 minutes of warm-up, 30 minutes of stabilization exercises, and 10 minutes of cool-down. Stabilization exercises will be selected from an exercise pool according to the individual's needs, with progression ensured 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.
Treatment:
Other: Exercise
Exercise, and Connective tissue massage
Experimental group
Description:
Each exercise session lasts 50 minutes, consisting of 10 minutes of warm-up, 30 minutes of stabilization exercises, and 10 minutes of cool-down. Stabilization exercises will be selected from an exercise pool according to the individual's needs, with progression ensured 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. In this group, in addition to these exercises, connective tissue massage will be applied, starting from the basic regions and gradually incorporating other regions.
Treatment:
Other: Exercise
Other: Connective tissue massage
Exercise, and Electro-physical modalities
Experimental group
Description:
Each exercise session lasts 50 minutes, consisting of 10 minutes of warm-up, 30 minutes of stabilization exercises, and 10 minutes of cool-down. Stabilization exercises will be selected from an exercise pool according to the individual's needs, with progression ensured 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. Also, the electrotherapy program consists of 20 minutes of infrared therapy, continuous ultrasound will be applied to the right and left sides for 7 minutes each at an intensity of 2 W/cm², and 20 minutes of conventional TENS will be administered to the painful area.
Treatment:
Other: Exercise
Other: Infrared therapy
Other: Conventional TENS
Other: Continuous ultrasound

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Burcu AKKURT, PhD

Data sourced from clinicaltrials.gov

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