NCT07644988

Brief Summary

Levator scapulae muscle tightness is a common cause of neck pain due to poor posture. This study compares two manual therapy techniques: Positional Release Technique (PRT) and Post Isometric Relaxation (PIR). The goal is to determine which technique is more effective at reducing pain, improving neck range of motion, and decreasing functional disability in patients with this condition. Participants will be randomly assigned to receive either PRT or PIR for 4 weeks

Trial Health

75
On Track

Trial Health Score

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

Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
1mo left

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Study Progress83%
Feb 2026Jul 2026

Study Start

First participant enrolled

February 15, 2026

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

June 8, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

June 12, 2026

Completed
3 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2026

Completed
25 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 10, 2026

Expected
Last Updated

June 12, 2026

Status Verified

June 1, 2026

Enrollment Period

4 months

First QC Date

June 8, 2026

Last Update Submit

June 8, 2026

Conditions

Keywords

levator scapulae tightnessPIR in levator scapule tightness

Outcome Measures

Primary Outcomes (1)

  • Change in Pain Intensity

    Measured using the Numeric Pain Rating Scale (NPRS). Participants rate their average neck pain on an 11-point scale where 0 = 'no pain' and 10 = 'worst imaginable pain'

    Baseline and at 4 weeks (post-intervention)

Secondary Outcomes (2)

  • Change in Cervical Range of Motion

    Baseline and at 4 weeks (post-intervention)

  • Change in Functional Disability

    Baseline and at 4 weeks (post-intervention)

Study Arms (2)

Positional Release Technique (PRT)

EXPERIMENTAL

Patient lies prone. The therapist palpates the levator scapulae and uses the far hand to translate the scapula upward and apply rotation. The superior angle of the scapula is tilted downward. This position is held for 90 seconds. 10 repetitions for 3 sets per session

Procedure: Positional Release Technique

Post Isometric Relaxation (PIR)

ACTIVE COMPARATOR

Patient lies supine. The therapist stabilizes the shoulder and supports the neck. The patient performs an isometric contraction by moving the head back against resistance for 10 seconds. After relaxation, a passive stretch is applied for 10 seconds. 10 repetitions for 3 sets per session.

Procedure: post isometric relaxation

Interventions

Patient lies prone. The therapist palpates the levator scapulae and uses the far hand to translate the scapula upward and apply rotation. The superior angle of the scapula is tilted downward. This position is held for 90 seconds. 10 repetitions for 3 sets per session.

Positional Release Technique (PRT)

Patient lies supine. The therapist stabilizes the shoulder and supports the neck. The patient performs an isometric contraction by moving the head back against resistance for 10 seconds. After relaxation, a passive stretch is applied for 10 seconds. 10 repetitions for 3 sets per session.

Post Isometric Relaxation (PIR)

Eligibility Criteria

Age25 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age between 25 to 40 years.
  • Both male and female.
  • Presence of a trigger point in levator scapulae (palpable tender spot with jump sign).
  • Score greater than 20% on the Neck Disability Index.
  • Unilateral non-specific neck pain.
  • Confirmation of trigger point via algometer.

You may not qualify if:

  • History of trauma or fracture to the scapula or cervical spine.
  • Pregnancy.
  • Previous cervical spine surgery.
  • Diagnosis of cancer, cardiac condition, or infectious disease.
  • Specific neck pathology (e.g., disc prolapse, nerve root compression, whiplash).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

the University of Faisalabad

Faisalabad, Punjab Province, 38000, Pakistan

Location

MeSH Terms

Conditions

Myofascial Pain Syndromes

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
Participants are unaware of which technique is theoretically superior. The outcome assessor measuring NPRS, ROM, and NDI will be blinded to group allocation
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
assistant professor

Study Record Dates

First Submitted

June 8, 2026

First Posted

June 12, 2026

Study Start

February 15, 2026

Primary Completion

June 15, 2026

Study Completion (Estimated)

July 10, 2026

Last Updated

June 12, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Locations