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Clinical Trials/CTRI/2022/09/046043
CTRI/2022/09/046043Not yet recruitingPhase 1/2

Comparison of Myofascial Trigger Point Dynamic Cupping and Myofascial Release Technique on Pain and Function of Chronic calf pain

Sagar Khurana1 site in 1 country77 target enrollmentStarted: September 30, 2022Last updated:
Conditions

Trial Snapshot

Phase
Phase 1/2
Status
Not yet recruiting
Sponsor
Enrollment
77
Locations
1
Primary Endpoint
Numeric Pain Rating Scale (NPRS)

Study Overview

Brief Summary

Ethical approval of this study will be taken from the student project committee and ethical committee of Maharishi Markandeshwar Institute of Physiotherapy and Rehabilitation. Study will be done in accordance with Helsinki declaration revised 2013 and the National Ethical Guidelines for Biomedical Research involving Human Participants, 2017.

Recruitment and Intervention:

The objective of the study is to find out the effectiveness of Cupping Therapy versus Myofascial Release Technique in patients with Chronic Calf Pain. Participants will be chosen from a group of 18-25 year-old who had been suffering from chronic calf pain for at least one trigger point in calf region. Each subject’s complete demographic information, including name, age, gender, weight, and height, will be recorded. For 3 weeks, treatment will be provided twice a week. The Numeric Pain Rating Scale and Pain Pressure Threshold (PPH) is used to assess pain intensity and Range of Motion and SF-36  Questionnaire is used to assess disability, and baseline measures will be done after the final intervention

Study Design

Study Type
Interventional
Allocation
Permuted block randomization, fixed
Masking
Not Applicable

Eligibility Criteria

Ages
18.00 Year(s) to 25.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •Adults(18-25years)
  • •At least one or more trigger points in the calf muscles.
  • •Both males and females.
  • •Muscles associated with trigger points must be soleus and gastrocnemius.
  • •Both limbs are given equal importance.

Exclusion Criteria

  • •Tumor, fracture, rheumatoid arthritis, osteoporosis, or any vascular condition in the lower limbs.
  • •Previous surgery in the affected leg below the hip.
  • •History of Deep vein thrombosis or varicose vein.
  • •Contraindication to Cupping Therapy.

Outcomes

Primary Outcomes

Numeric Pain Rating Scale (NPRS)

Time Frame: 2 times for 3 weeks

Pain Pressure Thershold (PPH)

Time Frame: 2 times for 3 weeks

Secondary Outcomes

  • Range of Motion of Ankle Joint(SF-36 Questionnaire)

Investigators

Sponsor
Sagar Khurana
Sponsor Class
Other [self]

Study Sites (1)

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