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Intracranial membrane release and Unwinding vs Suboccipital Release Technique in chronic neck pain. A Randomized Controlled Trial

Intracranial membrane release and Unwinding vs Suboccipital Release Technique on pain, disability & range of motion in chronic neck pain. A Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626000235303
Acronym
IMR (Intracranial membrane release)
Enrollment
160
Registered
2026-02-24
Start date
2026-04-06
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

A randomized controlled study aimed to evaluate the effectiveness of intracranial membrane release and unwinding in comparison to suboccipital release technique in chronic nonspecific neck pain. Intended Hypothesis: Intracranial membrane release and unwinding will be more effective than the suboccipital release technique in patients with chronic nonspecific neck pain.

Interventions

Patients fulfilling the inclusion criteria will be assigned to Group A or B randomly. Experimental group (Group A) will receive intracranial membrane release and unwinding while Control group (Group B) will receive suboccipital inhibition release and thermotherapy. The intervention will be provided for 3 days a week, 30 mins per session for 8 weeks. Experimental group (Group A): 1. Intracranial Membrane Release: A gentle pressure of 5 gram will be used and each treatment technique will be appli

Patients fulfilling the inclusion criteria will be assigned to Group A or B randomly. Experimental group (Group A) will receive intracranial membrane release and unwinding while Control group (Group B) will receive suboccipital inhibition release and thermotherapy. The intervention will be provided for 3 days a week, 30 mins per session for 8 weeks. Experimental group (Group A): 1. Intracranial Membrane Release: A gentle pressure of 5 gram will be used and each treatment technique will be applied for 5 mins. Patient will be in supine position. • Frontal Lift Technique (Anterior-Posterior Cranial Membrane Traction): The therapist will place ring and little fingers along the outer edges of the frontal bone, near the zygomatic processes while middle and index fingers are positioned adjacent to the midline of the frontal bone. Gentle posterior pressure will be applied using the index fingers on the midline, while the ring fingers will simultaneously move in an anterior and downward (caudal) direction. • Sphenoid Lift Technique (Anterior-Posterior Cranial Membrane Traction): The therapist places the index finger on the greater wing of the sphenoid bone, the middle finger on the pterion, the ring finger behind the ear over the asterion, and the little finger on the lateral angle of the occiput. Both thumbs will be placed together on the midline of the head. A gentle distraction force will be applied. • Parietal Lift Technique (Superior-Inferior Cranial Membrane Traction): The Therapist will be seated at the head of the patient placing the fingertips gently to contact the lateral aspects of the parietal bones while fifth fingers rest near asterion, avoiding pressure on temporal bones. Thumbs will cross but do not touch the patient’s scalp. A steady pressure will be maintained. • Temporal Ear Pull Technique (Transverse Cranial Membrane Traction): The therapist will place hands over the parietal and temporal bones. The therapist will gently palpate the temporal bones as they rock forward, backward, inward, and outward. The therapist will lightly grasp the earlobes with thumbs and forefingers on each side, applying gentle traction by pulling backward, downward, and apart to release tension in the cranial sutures. 2. Unwinding: The patient lies supine with their shoulders at the head of the table. The therapist will sit at the head of the table and holds the patient’s head. One hand will support the head, while the other will lightly hold the frontal bone. The head will be allowed to move naturally and spontaneously while resisting backtracking to encourage new movement patterns. The treatment will be applied for 5 mins. An independent assessor blinded to the treatment will assess all the patients for treatment outcome assessment at baseline, after 1st session, after 4th week and post treatment (i.e. post-completion of 8-week treatment program). Adherence to the intervention will be monitored by an independent assessor who is blinded to group allocation. The assessor will use standardized session attendance checklists to record participant attendance, session completion, and duration of participation without knowledge of the treatment condition. Session logs will be reviewed regularly by one of the co-investigators not involved in treatment allocation to ensure compliance with the intervention protocol. Any missed or incomplete sessions will be documented, along with reported reasons, to minimize assessment bias and enhance methodological validity.

Sponsors

Syeda Waniya Riaz, Iqra University
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

Patients having Chronic Nonspecific Neck Pain (CNSNP) for 3 months or more with at least moderate pain intensity of greater than or equal to 45 mm on a 100-mm Visual Analog Scale (VAS), willing to participate will be recruited.

Exclusion criteria

Exclusion criteria will be any history related to spinal surgery, previous administration of epidural injections. Patients having Neck Pain (NP) due to specific pathology, Patients with radiculopathy or myelopathy, Traumatic spinal cord injury and NP associated with progressive neurological deficit, loss of strength or having severe comorbid somatic and psychiatric disorders such as oncological diseases or major depression and current pregnancy

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 14, 2026