NCT06648070

Brief 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 .

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2024

Geographic Reach
1 country

1 active site

Status
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 Start

First participant enrolled

July 15, 2024

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

October 1, 2024

Completed
17 days until next milestone

First Posted

Study publicly available on registry

October 18, 2024

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2025

Completed
Last Updated

October 18, 2024

Status Verified

October 1, 2024

Enrollment Period

1 year

First QC Date

October 1, 2024

Last Update Submit

October 17, 2024

Conditions

Outcome Measures

Primary Outcomes (3)

  • Change in ROM

    ROM will be measured with goniometer

    2 weeks

  • Pain intensity

    It will be measured using Numeric pain rating scale

    2 weeks

  • Neck Disability

    It will be measured using Neck disability index

    2 weeks

Study Arms (2)

NMR Group

EXPERIMENTAL

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

PFS Group

EXPERIMENTAL

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

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.

NMR Group

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.

PFS Group

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

  • History of cervical spine
  • Fracture
  • Trauma to neck

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Foundation University College of Physical Therapy

Rawalpindi, Punjab Province, 46000, Pakistan

RECRUITING

MeSH Terms

Conditions

Oculocerebral hypopigmentation syndrome type Preus

Central Study Contacts

Hina Ayub, MS-MSKPT

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized Control Trial
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 1, 2024

First Posted

October 18, 2024

Study Start

July 15, 2024

Primary Completion

July 15, 2025

Study Completion

July 15, 2025

Last Updated

October 18, 2024

Record last verified: 2024-10

Locations