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Clinical Trials/NCT03419065
NCT03419065CompletedNot Applicable

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

Towson University2 sites in 1 country12 target enrollmentStarted: January 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
12
Locations
2
Primary Endpoint
Interview

Study Overview

Brief Summary

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

Detailed Description

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Pregnant women on bed rest for high risk pregnancy

Exclusion Criteria

  • Not provided

Arms & Interventions

Relaxation Intervention

Other

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

Intervention: Relaxation Intervention (Behavioral)

Outcomes

Primary Outcomes

Interview

Time Frame: 5-7 days

Participants participated in a follow up interview

Secondary Outcomes

  • Post-survey(5-7 days)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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