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RecruitingNCT06648070Updated Oct 18, 2024

"Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome Among IT Professionals

An interventional study of Neuromuscular reeducation technique and Post Facilitation Stretch in Upper Cross Syndrome, sponsored by Foundation University Islamabad. Recruiting at 1 site in Pakistan. Open to participants aged 20 Years to 40 Years. Per ClinicalTrials.gov, last updated 2024-10-18.

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

From the registry’s dates

  • Primary completion was expected by Jul 2025, 1 year 2 months ago, but the record still lists the study as recruiting.
  • Started Jul 2024; still recruiting 2 years 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
44
Allocation
Randomized
Ages
20 Years to 40 Years
Sex
All
01

Study summary

This study is a randomised control trial and the purpose of this study is to determine the "Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome among IT professionals .

Read the detailed description

The purpose of this study is to determine the "Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome among IT professionals

we make 2 groups control and treatment group . we give NMR technique to treatment group and PFS technique to control group in patients with upper cross syndrome.

first we take base line readings of cervical ROM , NPRS AND neck diasbilty index.

after 2 weeks of treatment again we take same readings and compare both readings.

with techniques we also perform strengthning excercise of weal muscles for both groups

02

Conditions studied

  • Upper Cross Syndrome

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03

In context

Syndrome

9,217 studies on the registry are indexed under Syndrome; 1,031 are open to participants now.

This study's planned enrollment of 44 is below the median of 50 across 6,515 interventional studies indexed under Syndrome.

Browse Syndrome 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
20 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • IT profressionals
  • 20 - 40 years
  • Both genders
  • Diagnosed UCS
  • Pain from 2 months
  • Minimum 4 - 6 hiurs working

Exclusion criteria

Exclusion criteria:

  • History of cervical spine
  • Fracture
  • Trauma to neck
05

Study design

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

Study arms

  • Experimental
    NMR Group

    On group A we will perform NEUROMUSCULAR REEDUCATION TECHNIQUE: we perform this technique on tight muscles which are: 1. levator scapulae 2. upper trapezius 3. pectoralis major

    Procedure: Neuromuscular reeducation technique

  • Experimental
    PFS Group

    On group B we perform POST FACILITATION STRETCH TECHNIQUE on tight muscles same as group A 1. levator scapulae 2. upper trapezius 3. pectoralis major

    Procedure: Post Facilitation Stretch

Interventions

  • ProcedureNeuromuscular reeducation technique

    5 repetitions of neuromuscular reeducation technique i.e. deep pressure along muscles origin to insertion with active movement of that muscle with 10 seconds rest of each repetitions. Control group will receive 3- 5 repetitions of Post Facilitation stretch to the tight muscles of UCS i.e. 20% maximal isometric contraction of the muscles to be stretched for 5-10 seconds followed by a rapid stretch ( through the new barrier) of 10 seconds. After stretch muscle is allowed to relax in mid range for 10 seconds.

  • ProcedurePost Facilitation Stretch

    3- 5 repetitions of Post Facilitation stretch to the tight muscles of UCS i.e. 20% maximal isometric contraction of the muscles to be stretched for 5-10 seconds followed by a rapid stretch ( through the new barrier) of 10 seconds. After stretch muscle is allowed to relax in mid range for 10 seconds.

06

What researchers measure

Primary outcomes

  1. Change in ROM

    ROM will be measured with goniometer

    Time frame: 2 weeks

  2. Pain intensity

    It will be measured using Numeric pain rating scale

    Time frame: 2 weeks

  3. Neck Disability

    It will be measured using Neck disability index

    Time frame: 2 weeks

07

Study locations

1 of 1 sites recruiting
  • Foundation University College of Physical Therapy
    Rawalpindi, Punjab 46000, Pakistan
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 18, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06648070
Lead sponsor
Foundation University Islamabad
Responsible party
Sponsor
First posted
Oct 18, 2024
Start date
Jul 15, 2024
Primary completion
Jul 15, 2025 (estimated)
Completion
Jul 15, 2025 (estimated)
Last update
Oct 18, 2024

Study contacts

Hina Ayub, MS-MSKPT
Contact
hinaayub881@gmail.com
03495830798

Oversight

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

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