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Suboccipital Release Versus Instrument- Assisted Soft Tissue Mobilization on Tension Type Headache

Cairo University (CU) logo

Cairo University (CU)

Status

Not yet enrolling

Conditions

Tension-Type Headache
Instrumental Assisted Soft Tissue Mobilization
Suboccipital Release

Treatments

Other: Instrument Assisted soft tissue mobilization
Other: conventional physical therapy program
Other: Suboccipital release

Study type

Interventional

Funder types

Other

Identifiers

NCT06703385
Nada-005491

Details and patient eligibility

About

The study aims to explore the impact of suboccipital release versus instrument-assisted soft tissue mobilization on pain intensity, pressure pain threshold, headache impact test, and headache frequency in patients with tension headache. The research will also examine the effects of these methods on headache impact tests and frequency.

Full description

Headache prevalence ranges from 38.2 to 59.4%, with a lifetime prevalence of 26.1-45%. Tension Type Headache can be episodic or chronic, with 78% occurring less than 15 times/month and 6% occurring more than 15 times/month. Tension Type Headache has a greater socioeconomic burden, leading to lower productivity and workday loss. Tension Type Headache is linked to myofascial pain and trigger points, which can cause sensory changes and reduced pain threshold. Studies show that referred pain from myofascial trigger points reproduces headache in patients with , leading to increased symptom severity. Frequent Episodic tension type headache increases the risk of developing chronic tension type headache due to analgesic overuse. instrumental assisted soft tissue mobilization, a physical therapy technique, promotes fascia realignment and reduces strain on the clinician's hands.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Participants of both gender will be between the ages of 18 and 60.

  2. Episodic tension type headache criteria, according to the International Headache Society's Headache Classification Committee., have at least two of the following characteristics.

    • Recurrent episodes of headache on less than 15 days per month for at least 3 months
    • Headache that last for from around 30 min till seven days.
    • At least 2 of the following features are found in a headache:
    • A location that is on two sides.
    • Tightening/pressing quality (non-pulsating).
    • Intensity is mild to moderate.
    • Both of the following: Not worsened by routine physical activity, there is no nausea or vomiting.
    • Only have one photophobia/ phonophobia
  3. Patients have active trigger points in suboccipital muscle and upper trapezius muscle

  4. The presence of myofascial trigger points was determined by therapist using the diagnostic criteria described by Simons .,(1999) ,The major criteria of active myofascial trigger points were: Regional neck pain, Pain or altered sensation in the expected distribution of referred pain from a myofascial trigger point, Taut band palpable in an accessible muscle.

Exclusion criteria

  1. Patients who have had a history of cancer
  2. Patients who have had cervical and cranial surgery
  3. Patients with severe psychological disorders (major Depression)
  4. Patients with uncontrolled hypertension
  5. Dysfunctions in the tempo-mandibular joint
  6. Headaches associated with high fever, stiff neck, or rash, problems of vision or profound dizziness
  7. Female who are pregnant or lactating

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 3 patient groups

conventional program
Active Comparator group
Description:
Twenty patients will receive conventional physical therapy including Hot pack and exercise therapy program (ROM exercise, stretching exercise, isometric strengthening exercise for cervical muscles
Treatment:
Other: conventional physical therapy program
suboccipital release
Experimental group
Description:
Twenty patients will receive suboccipital release plus the Same conventional physical therapy program.
Treatment:
Other: Suboccipital release
Other: conventional physical therapy program
instrumental assisted soft tissue mobilization
Experimental group
Description:
Twenty patients will receive instrumental assisted soft tissue mobilization plus the Sam conventional physical therapy program.
Treatment:
Other: conventional physical therapy program
Other: Instrument Assisted soft tissue mobilization

Trial contacts and locations

1

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Central trial contact

Nada Gamal Saad, physical therapist

Data sourced from clinicaltrials.gov

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