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Chronic Neck PainDMR-CNPNCT07761793

Diaphragmatic Myofascial Release Added to Neck Exercises for Chronic Neck Pain

A study testing Neck Exercise Program and Diaphragmatic Myofascial Release and Diaphragm-Directed Manual Therapy in people with Chronic Neck Pain, run by Abdelrahman Alghoul at 1 site in Palestinian Territories.

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Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

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Trial summary

Chronic neck pain can affect daily activities and may be associated with pain, disability, fear of movement, and fatigue. Exercise is commonly used to manage chronic neck pain, but some people continue to experience symptoms despite exercise treatment. Read more about this study

Who is it for?
Ages 25 to 60 years
Conditions the study is for
Chronic Neck Pain
What is being tested?
Neck Exercise Program and Diaphragmatic Myofascial Release and Diaphragm-Directed Manual Therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 sitePalestinian Territories
Study dates
Oct 2026to Jan 2027
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Men and women aged 25-60 years.
  • Diagnosis of chronic neck pain lasting longer than 3 months.
  • Ability to understand and follow instructions.

Who cannot join

  • Previous cervical spine surgery.
  • Cervical radiculopathy or myelopathy.
  • History of fracture, inflammatory disease, malignancy, or neurological disorder.
  • Respiratory diseases such as chronic obstructive pulmonary disease (COPD) or severe asthma.
  • Current vestibular disorder.
  • Pregnancy.
  • Receipt of physical therapy or manual therapy during the previous 3 months.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Abdelrahman Alghoul, BSc contact

+970595248697

a.s.alghoul98@gmail.com

Palestinian Territories1 site
  • Alnos Street

    Gaza

    Abdelrahman Alghoul, 0595248697, a.s.alghoul98@gmail.com

Other trials in Palestinian Territories

About this study

Official title: Effect of Adding Diaphragmatic Myofascial Release to a Neck Exercise Program on Pain, Disability, Fatigue, and Kinesiophobia Among Patients With Chronic Neck Pain in the Gaza Strip: A Randomized Controlled Trial

Chronic neck pain can affect daily activities and may be associated with pain, disability, fear of movement, and fatigue. Exercise is commonly used to manage chronic neck pain, but some people continue to experience symptoms despite exercise treatment.

This study will investigate whether adding diaphragmatic myofascial release, a hands-on manual therapy directed toward the diaphragm and surrounding tissues, to a neck exercise program provides greater benefits than neck exercises alone in adults with chronic neck pain.

Read more

Sixty adults aged 25 to 60 years with chronic neck pain lasting more than three months will be randomly assigned to one of two groups. The control group will receive a supervised neck exercise program, while the intervention group will receive the same neck exercise program combined with diaphragmatic myofascial release and related diaphragmatic manual therapy. Both groups will receive treatment for six weeks, with three supervised sessions per week.

Pain, neck-related disability, fear of movement, and fatigue will be assessed before treatment, immediately after the six-week intervention, and four weeks after completion of treatment. The study will examine whether adding diaphragmatic myofascial release to neck exercises leads to greater improvements in these outcomes compared with neck exercises alone.

Read the detailed description

This study is a prospective, assessor-blinded, parallel-group randomized controlled trial that will be conducted at the outpatient Physical Therapy Clinic of Nasser Medical Complex in the Gaza Strip. The study aims to evaluate the added effect of diaphragmatic myofascial release and diaphragm-directed manual therapy when combined with a standardized neck exercise program in adults with chronic neck pain.

Participants will be randomly allocated in a 1:1 ratio to either an intervention group or a control group using a computer-generated random sequence. The control group will receive a supervised neck exercise program that includes deep cervical flexor training, cervical stabilization, stretching, postural correction, scapular strengthening, and a home exercise program. The intervention group will receive the same neck exercise program in addition to a diaphragm-focused intervention that includes manual diaphragm release, diaphragmatic myofascial release, release of accessory respiratory muscles, and breathing re-education.

The intervention period will last six weeks, with three supervised treatment sessions per week. Outcomes will be assessed at baseline, immediately after the intervention, and at a four-week follow-up. The clinical outcomes include neck-related disability measured using the Neck Disability Index (NDI), pain intensity measured using the Numeric Pain Rating Scale (NPRS), kinesiophobia measured using the Tampa Scale of Kinesiophobia (TSK-17), and fatigue measured using the Fatigue Severity Scale (FSS).

The study will compare changes over time between the intervention and control groups to determine whether adding the diaphragmatic intervention to neck exercises provides additional benefits for patients with chronic neck pain.

Being tested
Neck Exercise Program, Diaphragmatic Myofascial Release and Diaphragm-Directed Manual Therapy
Keywords
Chronic Neck Pain, Diaphragmatic Myofascial Release, Neck Exercise, Manual Therapy, Physical Therapy, Kinesiophobia, Fatigue, Neck Disability, Pain Intensity, Diaphragmatic Breathing
Medical subject headings
Kinesiophobia, Fatigue, Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Neck Exercise ProgramOther

    A supervised neck exercise program including deep cervical flexor training, cervical stabilization exercises, stretching of the upper trapezius, levator scapulae, pectoralis major, and sternocleidomastoid muscles, postural correction exercises, scapular strengthening, and a daily home exercise program. Participants will attend 3 supervised sessions per week for 6 weeks.

  • Diaphragmatic Myofascial Release and Diaphragm-Directed Manual TherapyOther

    The diaphragm-focused intervention includes manual diaphragm release using gentle sustained traction under the lower costal margin during exhalation; diaphragmatic myofascial release targeting the lower ribs, xiphoid region, costal margins, and related fascial structures; manual release of accessory respiratory muscles including the sternocleidomastoid, scalenes, upper trapezius, and pectoralis minor; and diaphragmatic breathing re-education.

Study groups in NCT07761793
Study groupRoleWhat they receive
Neck Exercise ProgramActive comparatorParticipants will receive a supervised neck exercise program consisting of deep cervical flexor training, cervical stabilization exercises, stretching exercises, postural correction, scapular strengthening, and a home exercise program. The intervention will be provided for 6 weeks with 3 supervised sessions per week.
Receives: Other: Neck Exercise Program
Neck Exercise Program + Diaphragmatic InterventionExperimentalParticipants will receive the same supervised neck exercise program as the active comparator group, combined with a diaphragm-focused intervention consisting of manual diaphragm release, diaphragmatic myofascial release, release of accessory respiratory muscles, and breathing re-education. Treatment will be provided for 6 weeks with 3 supervised sessions per week.
Receives: Other: Neck Exercise Program; Other: Diaphragmatic Myofascial Release and Diaphragm-Directed Manual Therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Neck Disability Index (NDI) Score

    Neck-related disability will be assessed using the Neck Disability Index (NDI), a 10-item self-reported questionnaire assessing the impact of neck pain on daily functioning. Each item is scored from 0 to 5, producing a total score from 0 to 50, which can be expressed as a percentage from 0% to 100%. Higher scores indicate greater neck-related disability.

    Measured: Baseline, immediately after the 6-week intervention, and 4 weeks after completion of the intervention

  2. Change in Neck Disability Index (NDI) Score

    Neck-related disability will be assessed using the Neck Disability Index (NDI), a 10-item self-reported questionnaire assessing the impact of neck pain on daily functioning. Each item is scored from 0 to 5, producing a total score from 0 to 50, which can be expressed as a percentage from 0% to 100%. Higher scores indicate greater neck-related disability.

    Measured: Baseline, immediately after the 6-week intervention, and 4 weeks after completion of the intervention.

Secondary outcomes (3)
  1. Change in Tampa Scale of Kinesiophobia (TSK-17) Score

    Kinesiophobia will be assessed using the 17-item Tampa Scale of Kinesiophobia (TSK-17). Each item is rated on a 4-point Likert scale, with total scores ranging from 17 to 68. Higher scores indicate greater fear of movement or reinjury.

    Measured: Baseline, immediately after the 6-week intervention, and 4 weeks after completion of the intervention.

  2. Change in Numeric Pain Rating Scale (NPRS) Score

    Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS). Participants will rate their average neck pain over the previous week on an 11-point scale from 0 (no pain) to 10 (worst imaginable pain). Higher scores indicate greater pain intensity.

    Measured: Baseline, immediately after the 6-week intervention, and 4 weeks after completion of the intervention

  3. Change in Fatigue Severity Scale (FSS) Score

    Fatigue will be assessed using the 9-item Fatigue Severity Scale (FSS). Each item is rated from 1 to 7. The mean of the nine items will be calculated, resulting in a score from 1 to 7, with higher scores indicating greater fatigue severity.

    Measured: Baseline, immediately after the 6-week intervention, and 4 weeks after completion of the intervention.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Aug 2026
  2. Study startOct 2026 (estimated)
  3. Primary completionJan 2027 (estimated)
  4. Study completionJan 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07761793
Sponsor's protocol ID
ALGHOUL-DMR-CNP-2026
Acronym
DMR-CNP
Status last verified
Aug 2026
First submitted
8 Aug 2026
Last updated
12 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Ajimsha MS, Al-Mudahka NR, Al-Madzhar JA. Effectiveness of myofascial release: systematic review of randomized controlled trials. J Bodyw Mov Ther. 2015 Jan;19(1):102-12. doi: 10.1016/j.jbmt.2014.06.001. Epub 2014 Jun 13.

    PubMed 25603749
  • Tatsios PI, Grammatopoulou E, Dimitriadis Z, Koumantakis GA. The Effectiveness of Cervical Spine and Diaphragm Manual Therapy Combined with Breathing Re-Education Exercises on Musculoskeletal, Respiratory and Psychophysiological Outcomes in Patients with Non-Specific Chronic Neck Pain: A Randomized Controlled Trial. J Clin Med. 2026 May 31;15(11):4266. doi: 10.3390/jcm15114266.

    PubMed 42279128
  • Tatsios PI, Grammatopoulou E, Dimitriadis Z, Koumantakis GA. The Effectiveness of Manual Therapy in the Cervical Spine and Diaphragm, in Combination with Breathing Reeducation Exercises, in Patients with Non-Specific Chronic Neck Pain: Protocol for Development of Outcome Measures and a Randomized Controlled Trial. Diagnostics (Basel). 2022 Nov 4;12(11):2690. doi: 10.3390/diagnostics12112690.

    PubMed 36359533
  • Simoni G, Bozzolan M, Bonnini S, Grassi A, Zucchini A, Mazzanti C, Oliva D, Caterino F, Gallo A, Da Roit M. Effectiveness of standard cervical physiotherapy plus diaphragm manual therapy on pain in patients with chronic neck pain: A randomized controlled trial. J Bodyw Mov Ther. 2021 Apr;26:481-491. doi: 10.1016/j.jbmt.2020.12.032. Epub 2021 Feb 16.

    PubMed 33992285

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