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临床试验/NCT03419065
NCT03419065已完成不适用

Relaxation Interventions for Pre-term Mothers on Hospitalized Bed-Rest

Towson University2 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2012年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
12
试验地点
2
主要终点
Interview

研究概览

简要总结

The purpose of this study is to investigate the effects of participation in relaxation exercises on pregnant women who are hospitalized on bed-rest.

详细描述

Women, 18 or older, who consent to this study will participate in a preliminary interview. Study participants will then be trained in the use of progressive muscle relaxation and guided imagery for pregnancy. Participants will be issued a listening device and an audio file and asked to practice it on a daily basis while in the hospital.

Prior to discharge or delivery, the participant will be visited by a member of the research team who will conduct a follow-up interview. The interviews and the relaxation practice sessions will take between 30 and 45 minutes each. The interviews will be audio-recorded, although no identifying information about the participants will be recorded.

At the conclusion of the study, participants will be given a CD of the audio relaxation program and thanked for their participation in the study.

There is minimal risk anticipated in association with participation in this study. All information gained from this study will remain confidential and is for educational purposes only. Participants are entitled to terminate their participation in the study at any time.

It is hoped that the results of this study will provide information about an intervention that may be beneficial to women with high-risk pregnancies. It is also hoped that participation in the exercises will be enjoyable and/or beneficial to you in some way. The results of this study may be used to justify further studies or to influence the type of interventions offered in this or similar settings.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • Pregnant women on bed rest for high risk pregnancy

排除标准

  • 未提供

研究组 & 干预措施

Relaxation Intervention

Other

Women hospitalized on bed-rest for high risk pregnancy participated in Relaxation Interventions.

干预措施: Relaxation Intervention (Behavioral)

结局指标

主要结局

Interview

时间窗: 5-7 days

Participants participated in a follow up interview

次要结局

  • Post-survey(5-7 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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