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临床试验/NCT06057649
NCT06057649已完成不适用

Effects of Effleurage Abdominal Massage on Pain and Quality of Life in Primary Dysmenorrhea Among Female University Students in Lahore

University of Health Sciences Lahore2 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2024年4月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
52
试验地点
2
主要终点
Measure the level of Quality of Life

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

盲法说明

a third person will be involved as second assessor for blinding

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 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

排除标准

  • 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.

结局指标

主要结局

Measure the level of Quality of Life

时间窗: 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

时间窗: 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.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Aqeela Sarwar

Principal Investigator

University of Health Sciences Lahore

研究点 (2)

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