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Clinical Trials/CTRI/2025/07/090843
CTRI/2025/07/090843
Not yet recruiting
Not Applicable

Effect of Myofascial Release on Pain and Health Related Quality of Life in Women with Irregular Menstrual Cycle

Pakeeza Altaf1 site in 1 country28 target enrollmentStarted: July 25, 2025Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Pakeeza Altaf
Enrollment
28
Locations
1
Primary Endpoint
Visual Analogue Scale

Overview

Brief Summary

This study aims to investigate the impact of myofascial release (MFR) therapy on pain and overall health-related quality of life (HRQoL) in women experiencing irregular menstrual cycles. Irregular menstruation is often associated with dysmenorrhea (painful menstruation), mood disturbances, and other symptoms that negatively affect daily functioning and quality of life. Myofascial release, a manual therapy technique that targets muscle tension and fascia, has shown potential in alleviating pain and improving mobility. This study will assess whether MFR can reduce menstrual pain, enhance physical and emotional well-being, and improve general quality of life in women with irregular cycles. The outcomes will be measured through pain intensity scales and HRQoL assessments, including physical, mental, and emotional health components.

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 45.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • Female participant Typically, between 18 to 45 years Diagnosed with irregular menstrual cycle Experience of menstrual related pain or pelvic pain Ability to commit to the study duration and procedures.

Exclusion Criteria

  • Any severe underlying conditions Recent use of hormonal therapies or surgical interventions related to menstrual cycles Pre-existing conditions affecting the musculoskeletal system that may interfere with myofascial release treatment Mental health issues that might affect participation or reporting of outcomes Pregnant or breastfeeding women.

Outcomes

Primary Outcomes

Visual Analogue Scale

Time Frame: Baseline and at the end of 4th week

Numeric Pain Rating Scale

Time Frame: Baseline and at the end of 4th week

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Pakeeza Altaf
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Pakeeza Altaf

Maharishi Markandeshwar Institute of Physiotherapy and Rehabilitation

Study Sites (1)

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