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Taping and PMR Effects in Primary Dysmenorrhea

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

Condition(s)Dysmenorrhea Primary
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryThe 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 incorpora
Who can participateInclusion 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
Ages18 Years to 25 Years
SexFemale
Lead sponsorRiphah International University
LocationsLahore, Punjab Province, Pakistan
Start date2023-12-23
NCT IDNCT06761755
Official listinghttps://clinicaltrials.gov/study/NCT06761755

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