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CompletedNCT05063890Updated Oct 1, 2021

Comparison of Muscle Specific and Movement Specific Muscle Energy Technique in the Management of Mechanical Neck Pain: a Randomized Controlled Trial.

An interventional study of Muscle Specific Post Isometric Relaxation MET and Movement Specific Post Isometric Relaxation MET in Neck Pain, sponsored by Foundation University Islamabad. Completed at 1 site in Pakistan. Open to participants aged 19 Years to 44 Years. Per ClinicalTrials.gov, last updated 2021-10-01.

Sponsored by Foundation University Islamabad · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 years 5 months after the study started (first participant enrolled Apr 2017, registered Sep 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
66
Allocation
Randomized
Ages
19 Years to 44 Years
Sex
All
01

Study summary

the purpose of this study is to compare the effects of muscle-specific muscle energy technique and movement-specific muscle energy technique in terms of pain, function and cervical range of motion in persons with mechanical neck pain.

02

Conditions studied

  • Neck Pain

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Keywords

  • neck pain
03

In context

Neck Pain

1,232 studies on the registry are indexed under Neck Pain; 255 are open to participants now.

This study's enrollment of 66 is above the median of 52 across 1,004 interventional studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

Foundation University Islamabad is the lead sponsor of 238 studies on the registry; 128 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 44 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Mechanical neck pain ranging from 40-80 mm on visual analogue scale (VAS) Age between 19-44 years Pain or limitation on cervical motion

Exclusion criteria

-

Exclusion Criteria:

History of fracture, surgery or trauma in the neck Cervical radiculopathy Myelopathy Spondylosis Syringomyelia Thoracic outlet syndrome Infection Malignancy Inflammatory or rheumatic disorders Vascular syndromes

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
66 participants (actual)

Study arms

  • Experimental
    Muscle Specific MET

    Procedure: Muscle Specific Post Isometric Relaxation MET · Procedure: unilateral postero-anterior glide · Procedure: Heating and TENS

  • Experimental
    Movement specific MET

    Procedure: Movement Specific Post Isometric Relaxation MET · Procedure: unilateral postero-anterior glide · Procedure: Heating and TENS

Interventions

  • ProcedureMuscle Specific Post Isometric Relaxation MET

    3-5 reps of Post Isometric Relaxation MET targeted at muscles of the neck prone to get short

  • ProcedureMovement Specific Post Isometric Relaxation MET

    3-5 reps of Post Isometric Relaxation MET targeted at specific movements of the cervical spine

  • Procedureunilateral postero-anterior glide

    3 sets of unilateral posteroanterior glide (10-15 oscillations) at the involved segment

  • ProcedureHeating and TENS

    Heating and TENS for 10 minutes

06

What researchers measure

Primary outcomes

  1. Visual Analogue Scale

    Pain will be measured using Visual Analogue Scale, with greater score signifying greater pain

    Time frame: 5 days

  2. Neck Disability Index

    Function and neck related disability will be measured using Neck Disability Index, with greater score signifying greater disability and poorer outcome

    Time frame: 5 days

  3. Cervical Range of Motion

    Cervical Range of Motion will be measured using a universal goniometer, with greater score signifying more favorable outcome

    Time frame: 5 days

07

Study locations

1 site
  • Foundation University Institute of Rehabilitation Sciences.
    Islamabad, Federal 46000, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 1, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05063890
Lead sponsor
Foundation University Islamabad
Responsible party
Sponsor
First posted
Oct 1, 2021
Start date
Apr 1, 2017
Primary completion
Jan 30, 2019
Completion
Jan 30, 2019
Last update
Oct 1, 2021

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2021. You cannot join it, but the record below documents what was studied.

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