Effects of Effleurage Abdominal Massage on Pain and Quality of Life in Primary Dysmenorrhea Among Female University Students in Lahore
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 52
- Locations
- 1
- Primary Endpoint
- Measure the level of Quality of Life
Study Overview
Brief Summary
To find out the answer of the study question that effleurage abdominal massage has any effect on pain and quality of life in primary dysmenorrhea among university students or nota study will be conducted with an objective to evaluate the effects of effleurage abdominal massage on pain and quality of life in primary dysmenorrhea among university students
Detailed Description
Primary dysmenorrhea, the commonly occurring gynecological issue faced by young girls. It severely affects quality of female life. It leads to fatigue, psychological issues, lack of interest in selfcare and daily activities that results in absenteeism at work and educational institutes. It also badly affects academic performance and extra-curricular activities. Different pharmacological and non-pharmacological interventions are being used for reducing its negative effects, such as effleurage abdominal massage intend to decrease the problems faced by students as a result of this frightening issue. Here the question arises for health professionals that effleurage abdominal massage has any effect on pain and quality of life in primary dysmenorrhea among university students or not? To find out the answer of this question a study will be conducted with an objective to evaluate the effects of effleurage abdominal massage on pain and quality of life in primary dysmenorrhea among university students. This study holds considerable implications in addressing potential adverse effects associated with pharmacological analgesic agents, thereby mitigating pain, lack of interest in work and enhancing functional capacity, hence improving quality of life. Moreover, it is anticipated to contribute to the reduction of healthcare costs.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- Single (Outcomes Assessor)
Masking Description
a third person will be involved as second assessor for blinding
Eligibility Criteria
- Ages
- 18 Years to 25 Years (Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Unmarried female university students from Lahore
- •Aged between 18-25 years
- •Diagnosed patients by gynecologist with primary dysmenorrhea for three previous consecutive cycles.
- •Regular menstrual cycles ranging 21-35 days lasting for 3-7 days.
- •Having pain score of 6 or more than 6 on Numeric Pain Rating Scale
Exclusion Criteria
- •Presence of any known abdominal or pelvic disease.
- •Obstructive vaginal or uterine congenital anomalies.
- •Presence of known or suspected secondary dysmenorrhea.
- •History of major abdominal or pelvic surgery in the previous three months.
- •History of hormonal therapy in the last six months.
- •History of using analgesics during menstruation.
- •History of having any medical disease i.e. cardiac and renal disease.
- •Participants doing regular exercise.
Arms & Interventions
experimental
Participants of experimental group will perform effleurage abdominal massage
Intervention: Effleurage Abdominal Massage (Other)
control
participants of control group will receive no intervention. they will be instructed to continue with their routine practices
Outcomes
Primary Outcomes
Measure the level of Quality of Life
Time Frame: 3 months
Outcome Measurement Tool: Euroqol-5D-5L scale for Quality of Life: The EQ-5D-5L scale will be used to assess students' quality of life across five dimensions and will allow respondents to indicate their level of functioning or health in each dimension with 1 as highest and 5 as lowest for each dimension. Additionally, EQ-5D-5L includes a visual analog scale (VAS) that will allow respondents to rate their overall health on a scale from 0 (worst imaginable health) to 100 (best imaginable health).
Measurement of Dysmenorrhea Induced Pain intensity
Time Frame: 3 months
Outcome Measurement Tool: Numeric Pain Rating Scale: Dysmenorrhea induced pain intensity measured by Numerical pain rating scale will be used having numbers from 0 to 10 to indicate the intensity of pain. Here is a breakdown of the numeric rating pain scale * 0: No pain. * 1-3: Mild pain. * 4-6: Moderate pain. * 7-9: Severe pain. * 10: Excruciating pain.
Secondary Outcomes
No secondary outcomes reported
Investigators
Aqeela Sarwar
Principal Investigator
University of Health Sciences Lahore