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NCT Number: NCT06686290

Effects of Post-Isometric Relaxation Versus Static Stretching in Patients With Levator Scapulae Syndrome.

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.

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Key information

Age range

24 year–59 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tehsil Headquarter Hospital Daska

Daska Kalan, Punjab Province, Pakistan

Location status: Recruiting

Location contact

Aiman Tariq, DPT

PRINCIPAL_INVESTIGATOR

Ali Raza, DPT

CONTACT

[email protected]

03326099065

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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 3.
  • 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.
  • Cancer.
  • Traumatic neck injury.
  • Previous cognitive and functional disorders.
  • Coagulopathy(

Treatment and study plan

Post-Isometric Relaxation Technique

Other

Post isometric 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.

Static Stretching

Other

Static Stretching

Primary outcomes

  1. Pain Level

    Time frame: Pre & Post 6 weeks

    Numeric Pain Rating Scale

  2. Disability Level

    Time frame: Pre & Post 6 weeks

    Neck Disability Index

  3. Range of Motion

    Time frame: Pre & Post 6 weeks

    Goniometer

  4. Muscle Length

    Time frame: Pre & Post 6 weeks

    Levator Scapulae Index

Study contacts

Contact information is provided by the study sponsor or research team.

Imran Amjad, Phd PT

CONTACT

[email protected]

03324390125

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Nov 13, 2024
Registry last updated
Nov 13, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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