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临床试验/CTRI/2024/10/075588
CTRI/2024/10/075588
招募中
不适用

Assessing the Accessibility and Efficacy of Telehealth Physiotherapy in Dysmenorrhea management A Qualitative outcome measure study

Galgotias University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年10月31日最近更新:

概览

阶段
不适用
状态
招募中
发起方
Galgotias University
入组人数
60
试验地点
1
主要终点
Visual Analog Scale

概览

简要总结

The study aims to assess the accessibility and efficacy of telehealth physiotherapy in managing dysmenorrhea. There are two groups of patients Group A and Group B. Participants in group A will receive physiotherapy sessions via a telehealth platform. Each session will last approximately 30 to 45 minutes and will include a combination of guided exercises, pain management techniques like TENS, heat therapy and educational components focused on lifestyle modifications to manage dysmenorrhea. Sessions will be conducted twice a week for a duration of 4 weeks. Participants will also have access to instructional videos and resources through the telehealth platform Whereas participants in group B will attend in person physiotherapy sessions at a designated clinic. The content and structure of these sessions will mirror those of the telehealth group, including similar exercises and pain management techniques like TENS , Heat therapy. In-person sessions will also occur twice a week for 4 weeks. By comparing patient reported pain levels functional mobility and overall quality of life before and after telehealth interventions using Oswestry Disability Index, Patient reported outcome measurement Information system PROMIS, this research seeks to evaluate the effectiveness of telehealth physiotherapy in alleviating dysmenorrhea symptoms.

Keywords Telehealth Physiotherapy, Dysmenorrhea Management, Accessibility, Efficacy, Telemedicine, Menstrual Pain

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 45.00 Year(s)(—)
性别
Female

入选标准

  • Females aged 18 to 45years who have been clinically diagnosed with primary dysmenorrhea.
  • Participants who experience moderate to severe menstrual pain defined as a score of 4 or higher on the Visual Analog Scale.
  • Participants who have access to the necessary technology like smartphone, tablet, or computer with internet access for telehealth sessions.

排除标准

  • Underlying pelvic pathologies Participants currently undergoing other forms of treatment for dysmenorrhea such as acupuncture or chiropractic care.
  • Those who are pregnant or planning to become pregnant during the study period.
  • The exclusion criterion was a failure to agree to participate in the study.

结局指标

主要结局

Visual Analog Scale

时间窗: baseline and 4 weeks

Oswestry Disability Index

时间窗: baseline and 4 weeks

Patient reported outcome measurement Information system PROMIS

时间窗: baseline and 4 weeks

次要结局

  • Working Ability, Location, Intensity, Days of Pain, Dysmenorrhea WaLIDD(Baseline and 4weeks)

研究者

发起方
Galgotias University
申办方类型
Research institution
责任方
Principal Investigator
主要研究者

Surbhi

Galgotias University

研究点 (1)

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