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Clinical Trials/NCT06761755
NCT06761755
Recruiting
Not Applicable

Combined Effects of Kinesiology Taping and Progressive Muscle Relaxation Technique on Pain, Anxiety and Body Awareness in Primary Dysmenorrhea

Riphah International University1 site in 1 country30 target enrollmentDecember 23, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dysmenorrhea Primary
Sponsor
Riphah International University
Enrollment
30
Locations
1
Primary Endpoint
numerical pain rating scale
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The study is randomized controlled trial,The study conducted in two groups. Group A has given the kinesiology taping on the lower abdomen and back for 1-3 days with progressive muscle relaxation technique for 10-20 minutes and a baseline treatment hot pack at a time twice a day from the start of menstruation and Group B has receive the kinesiology taping on the lower abdomen and baseline treatment hot pack without progressive muscle relaxation technique for 1-3 days. The total treatment duration will be 6 weeks. The rationale of this study is to provide empirical evidence regarding the efficacy and safety of kinesiology taping and progressive muscle relaxation. By investigating the potential benefits of this intervention, healthcare professionals can make informed decisions about incorporating K-taping and PMR in primary dysmenorhea. Focusing on the impact of kinesiology taping and progressive muscle relaxation on pain,anxiety, and body awareness aligns with a patient-centered approach to care. The goal is not only to reduce symptoms but also to enhance overall well-being and functional capacity

Detailed Description

The literature gap of the study is that upto our knowledge, there is little or no evidence found in previous researches on the combined effects of kinesiology taping in combination with progressive muscle relaxation technique in primary dysmenorrhea.

Registry
clinicaltrials.gov
Start Date
December 23, 2023
End Date
February 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • • Aged between 18-25 years
  • Unmarried female
  • Taking ≥4 points from Visual Analog Scale during menstrual cycle
  • Had moderate menstrual pain as measured by WaLLID score

Exclusion Criteria

  • • Complaints of low back pain due to any other pathology, any skin infection, sensitive skin or allergic to Kinesio Tape.
  • PCOD, Uterine/ ovarian tumor, Acute/ chronic pelvic pathology like PID, endometriosis, spinal pathology and deformity
  • Endometrial polyp, having a pelvic infection, using an intrauterine device, having venous congestion in the internal genital organs.
  • Who take analgesic

Outcomes

Primary Outcomes

numerical pain rating scale

Time Frame: 1st day

changes from base line NPRS is used to access the pain at 1st day or before the start of menstruation at the end score is calculated by dividing the obtained score by total 0 means no pain and 10 is maximum

STAI tool (state triate anxiety inventory)

Time Frame: 1st day

changes in the baseline ,STAI tool to access the anxiety of the patient feels at the start of menstruation at the end the score is calculated by dividing the score by total 0 means no anxiety and 4 means maximum anxiety

Body awareness questionaire

Time Frame: 1st day

Changes in the baseline, Body Awareness Questionnaire (Shields, Mallory \& Simon, 1989) acess the body awarenss during dysmenorhea , at the end the score is calcuted 0 means not true of me and 7 is the maximum true of me

Secondary Outcomes

  • Wallid questionaire(1st day)

Study Sites (1)

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