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Clinical Trials/NCT06686290
NCT06686290RecruitingNot Applicable

Effects of Post-Isometric Relaxation Versus Static Stretching on Pain, Range of Motion, Disability and Muscle Length in Patients With Levator Scapulae Syndrome.

Riphah International University1 site in 1 country42 target enrollmentStarted: April 24, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
42
Locations
1
Primary Endpoint
Pain Level

Study Overview

Brief Summary

Group A will be treated with Postisometric relaxation technique and Group B will be treated with Static stretching technique. Postisometric relaxation will be performed with the frequency of 5 times, such that it includes (30 isometric contraction of the muscle to be stretched for 10 seconds, followed by rest period of 5 seconds and then a stretch of 10 seconds hold. Stretching exercise will be performed with 30 second hold and with 5 repetitions. All Exercises will be performed 3 times per week for total of 4 weeks. Outcome measures will be conducted through pain, range of motion, disability and muscle length after 4 weeks.

Detailed Description

A Randomized Clinical Trial will be conducted at Tehsil Head Quarter Hospital Daska through consecutive sampling technique on 42 patients which will be allocated using computer generated sampling (random number table) into Group A and Group B. Group A will be treated with Postisometric relaxation technique and Group B will be treated with Static stretching technique. Postisometric relaxation will be performed with the frequency of 5 times, such that it includes (30 isometric contraction of the muscle to be stretched for 10 seconds, followed by rest period of 5 seconds and then a stretch of 10 seconds hold. Stretching exercise will be performed with 30 second hold and with 5 repetitions. All Exercises will be performed 3 times per week for total of 4 weeks. Outcome measures will be conducted through pain, range of motion, disability and muscle length after 4 weeks. Data will be analyzed during SPSS software version 25. The normality of data will be assessed by Shapiro-wilk test after which it will be decided either parametric or non-parametric test will be used within a group or between two groups.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Outcomes Assessor)

Masking Description

Assessor Blinded

Eligibility Criteria

Ages
24 Years to 59 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Both males and females.
  • •Age range of 24-59 years.
  • •Neck and medial border scapular pain for at least 3 months.
  • •NPRS score greater than
  • •Reduced side flexion and rotation of neck.
  • •Symptoms persisted for at least 3 months.
  • •Positive levator scapulae length test.
  • •Have suffered from myofascial pain

Exclusion Criteria

  • •Neuropathies.
  • •Vertebral fractures.
  • •Pregnancy.
  • •Fibromyalgia.
  • •Traumatic neck injury.
  • •Previous cognitive and functional disorders.
  • •Coagulopathy(

Arms & Interventions

Post Isometric Relaxation Technique

Experimental

Postisometric relaxation will be performed with the frequency of 5 times, such that it includes 30 isometric contraction of the muscle to be stretched for 10 seconds, followed by rest period of 5 seconds and then a stretch of 10 seconds hold.

Intervention: Post-Isometric Relaxation Technique (Other)

Static Stretching

Experimental

Stretching exercise will be performed with 30 second hold and with 5 repetitions. All Exercises will be performed 3 times per week for total of 4 weeks.

Intervention: Static Stretching (Other)

Outcomes

Primary Outcomes

Pain Level

Time Frame: Pre & Post 6 weeks

Numeric Pain Rating Scale

Disability Level

Time Frame: Pre & Post 6 weeks

Neck Disability Index

Range of Motion

Time Frame: Pre & Post 6 weeks

Goniometer

Muscle Length

Time Frame: Pre & Post 6 weeks

Levator Scapulae Index

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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