NCT07310823

Brief Summary

This study aims to investigate immediate and short-term effect of combining suboccipital myofascial release with Maitland mobilization techniques on headache intensity, duration, and frequency, CFRT, upper cervical ROM, general neck mobility, and PPT of upper trapezius and suboccipital muscles.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
57

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 16, 2025

Completed
4 days until next milestone

Study Start

First participant enrolled

December 20, 2025

Completed
10 days until next milestone

First Posted

Study publicly available on registry

December 30, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 30, 2026

Completed
2 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2026

Completed
Last Updated

December 30, 2025

Status Verified

December 1, 2025

Enrollment Period

1 month

First QC Date

December 16, 2025

Last Update Submit

December 16, 2025

Conditions

Keywords

cervicogenic headachesuboccipital myofacial releasemaitland mobilizationneck painCROM

Outcome Measures

Primary Outcomes (1)

  • headache intensity

    headache intensity Description: headache intensity which represent the primary outcome by using numerical analogue scale for measure intensity before treatment and one week post treatment

    Time Frame: before treatment and one week after treatment

Secondary Outcomes (1)

  • Headache Frequency Headache Duration Cervical Flexion Rotation Test Neck Mobility Assessment Pressure Pain Threshold

    Headache Frequency and headache duration before and one week after treatment. Cervical Flexion Rotation Test and Mobility Assessment and Pressure Pain Threshold measurement before and after and one week post treatment

Study Arms (3)

Group A (Suboccipital Myofascial Release)

ACTIVE COMPARATOR

Patients in this group will receive suboccipital myofascial release therapy for one session.

Other: suboccipital myofacial release

Group B (Maitland Mobilization)

ACTIVE COMPARATOR

Patients in this group will receive Maitland mobilization therapy for one session.

Other: maitland mobilization

Group C (Combined Group)

ACTIVE COMPARATOR

Patients in this group will receive both techniques; suboccipital myofascial release therapy then Maitland mobilization for one session.

Other: combined myofacsial release with maitland mobilization

Interventions

one session of myofacial release for suboccipital muscle

Group A (Suboccipital Myofascial Release)

one session of upper cervical vertebral grade one and two mobilization

Group B (Maitland Mobilization)

one session of myofacsial release and maitland mobilization for upper cervical and suboccipital muscle

Group C (Combined Group)

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Each patient will be included in our study if only he/she meets all of the following criteria:
  • Age between 20- 40 year.
  • No physiotherapy intervention at least for the last three months (Mohamed et al., 2019).
  • Neck pain elicited and disturbed by neck movement or maintained position pain produced by pressure over upper cervical (Dunning et al.,2021).
  • Limited neck motion with flexion and rotation test less than or equal 32 degree on both right and left side (Dunning et al.,2021).
  • Patients suffered from intermittent headaches of varying duration and pain level at least once every week through the last 3 months (Hall et al., 2010; Khalil., et al 2019).
  • The patient will be excluded if he /she meets one of the following criteria:
  • Physical therapy intervention during last three months (Mohamed et al., 2019).
  • Primary headaches such as migraine or tension type headache (Mohammadi et al.,2021).
  • Cervical radiculopathy, history of neck trauma and previous surgery at neck or shoulder, spondylosis (Mohammadi et al.,2021).
  • Vertebrobasilar insufficiency or vestibular dysfunctions (Mohamed et al., 2019).
  • Any degenerative vertebral lesion (Shabbir et al., 2021).
  • Concomitant medical diagnosis of any primary headache (tension type or migraine) (Shabbir et al., 2021).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cairo university faculty of physical therapy

Giza, Egypt

Location

Related Publications (3)

  • Verma S, Tripathi M, Chandra PS. Cervicogenic Headache: Current Perspectives. Neurol India. 2021 Mar-Apr;69(Supplement):S194-S198. doi: 10.4103/0028-3886.315992.

  • Priyanka, D. A. T. (2023). A Literature Review to Find the Effectiveness of Suboccipital Myofascial Release Technique in Reducing Cervicogenic Headache. Int J Sci Res, 12(4).

    RESULT
  • Lerner-Lentz A, O'Halloran B, Donaldson M, Cleland JA. Pragmatic application of manipulation versus mobilization to the upper segments of the cervical spine plus exercise for treatment of cervicogenic headache: a randomized clinical trial. J Man Manip Ther. 2021 Oct;29(5):267-275. doi: 10.1080/10669817.2020.1834322. Epub 2020 Nov 5.

MeSH Terms

Conditions

Post-Traumatic HeadacheNeck Pain

Condition Hierarchy (Ancestors)

Headache Disorders, SecondaryHeadache DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • . MAHA MOSTAFA MOHAMMED ALIBEINY, ASS.PROF

    cairo uneversity faculty of physical therapy

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: A randomized controlled trial in which patients will be randomly assigned into three equal groups (19 patients per group) via the RANDOM.ORG method. Each group will receive a specific physical therapy management according the following: * Group A (Suboccipital Myofascial Release): Patients in this group will receive suboccipital myofascial release therapy for one session. * Group B (Maitland Mobilization): Patients in this group will receive Maitland mobilization therapy for one session. * Group C (Combined Group): Patients in this group will receive both techniques; suboccipital myofascial release therapy then Maitland mobilization for one session.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Msc candidate, orthopedic physical therapy department , cairo university

Study Record Dates

First Submitted

December 16, 2025

First Posted

December 30, 2025

Study Start

December 20, 2025

Primary Completion

January 30, 2026

Study Completion

February 1, 2026

Last Updated

December 30, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations