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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-40
SponsorFoundation University Islamabad

About this trial

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 .

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

IT profressionals

20 - 40 years

Both genders

Diagnosed UCS

Disqualifiers

History of cervical spine

Fracture

Trauma to neck

Trial design

Design model

Parallel

Treatments tested in this trial

  • Neuromuscular reeducation technique

    Procedure/Surgery

    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.

  • Post Facilitation Stretch

    Procedure/Surgery

    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.

Treatment groups

44 Participants
are divided into 2 treatment groups
Group A: NMR GroupExperimental treatment 1 intervention
Group B: PFS GroupExperimental treatment 1 intervention

Trial outcomes

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

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.