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NCT Number: NCT07477145

Effect of Body Mind Exercises and Specific Neck Exercises in Chronic Mechanical Neck Pain

To investigate the effect of body mind exercise and specific neck exercises in chronic mechanical neck pain on neck pain severity, functional disability, neck flexion range of motion, isometric neck muscle strength and quality of life.

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Key information

Age range

50 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Chronic mechanical neck pain is one of the most common musculoskeletal disorders affecting middle-aged and older adults and is associated with pain, reduced cervical mobility, functional disability, and decreased quality of life. Exercise therapy is widely recommended as a first-line conservative treatment for chronic neck pain. Previous studies have shown that both specific neck exercises and general physical activity can reduce pain and improve functional outcomes.

Body-mind exercises, which combine physical movement with focused attention and breathing control, may provide additional benefits by improving both physical and psychological aspects of chronic pain. However, the comparative effectiveness of body-mind exercises and specific neck exercises when combined with conventional physical therapy remains unclear.

The aim of this randomized controlled trial is to investigate the effect of body-mind exercises and specific neck exercises on pain intensity, functional disability, cervical range of motion, isometric neck muscle strength, and quality of life in individuals with chronic mechanical neck pain.

A total of 80 participants aged 50 to 65 years with chronic mechanical neck pain will be recruited and randomly allocated into four groups using a parallel-group design. Group A will receive conventional physical therapy alone. Group B will receive conventional physical therapy combined with body-mind exercises in the form of mindful aerobic treadmill walking. Group C will receive conventional physical therapy combined with specific cervical and scapular stabilization exercises. Group D will receive a combination of conventional physical therapy, body-mind exercises, and specific neck exercises.

All interventions will be performed over a treatment period of six weeks. Outcome measures will include pain intensity measured by the Numeric Pain Rating Scale (NPRS), functional disability assessed by the Neck Disability Index (NDI), cervical range of motion measured using a Cervical Range of Motion (CROM) device, isometric neck muscle strength measured using a handheld dynamometer, and quality of life assessed using the RAND-36 Health Survey. Measurements will be taken before the intervention and after completion of the six-week treatment period.

The results of this study will help determine the most effective exercise approach for improving clinical outcomes in patients with chronic mechanical neck pain and may provide evidence to guide physical therapy practice.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged between 50-65 years
  • Diagnosis of chronic mechanical neck pain (pain duration ≥ 3 months)
  • Pain intensity of at least 3/10 on the NPRS

Exclusion criteria

  • History of cervical surgery
  • Specific neck conditions (fractures, neoplasm, infection)
  • Pregnancy
  • Severe cardiopulmonary disease or other systemic illness affecting participation

Treatment and study plan

Conventional physical therapy group.

Behavioral

conventional therapy which includes: heat therapy (infrared) for 10 minutes, massage therapy 10 min, stretching of neck (Scalene, SCM, UFT, Levator scapulae) and pectoral muscles 20 min.

Body mind exercises group (mindful aerobic exercises)

Behavioral

Group B will receive conventional physical therapy (infrared, massage, and neck stretching) in addition to Body mind exercises (mindful aerobic exercises). The aerobic exercise will be performed at an intensity of at least 60% of maximal oxygen consumption (VO₂ max) to effectively improve cardiorespiratory fitness. The program will include treadmill walking 30 minutes.

specific neck exercise group

Behavioral

Group C will receive conventional therapy in addition to specific neck exercises. Specific exercises will include: cervical and scapular stabilization exercises.

Combined exercise group.

Behavioral

Group D will receive conventional therapy in addition to mindful aerobic exercises, cervical and scapular stabilization exercises.

Primary outcomes

  1. Pain Intensity

    Time frame: (pre-intervention) and after 6 weeks (post-intervention).

    Numeric Pain Rating Scale (NPRS, Arabic version) 0-10 scale; validated for Arabic-speaking populations (Alghadir et al., 2016)

  2. Quality of Life Measured by RAND-36 Health Survey

    Time frame: (pre-intervention) and after 6 weeks (post-intervention).

    Measures physical, emotional, and social functioning .

  3. Functional Disability

    Time frame: (pre-intervention) and after 6 weeks (post-intervention).

    Neck Disability Index (NDI, Arabic version) 10-item questionnaire.

  4. Cervical ROM

    Time frame: (pre-intervention) and after 6 weeks (post-intervention).

    CROM device. Measures flexion, extension, lateral flexion, rotation; 3 repetitions per movement (Kiatkulanusorn et al., 2023).

  5. Isometric Neck Strength

    Time frame: (pre-intervention) and after 6 weeks (post-intervention).

    Handheld dynamometer (HHD) Flexion (forehead), Extension (occiput), 3 maximal contractions of 5 sec each, average recorded (Ghamkhar et al., 2011)

Study contacts

Contact information is provided by the study sponsor or research team.

RAMY I KOMIR, MSc

CONTACT

[email protected]

+966553277511

RAMY I KOMIR, MSc

CONTACT

[email protected]

+966566060994

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Acronym: BME-SNE

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 17, 2026
Registry last updated
Mar 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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