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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03419065
Enrollment
12
Registered
2018-02-01
Start date
2012-01-01
Completion date
2013-06-01
Last updated
2018-02-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High Risk Pregnancy

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. All data collected from the research will remain confidential. Data collected from participants will immediately be assigned an identification number so that no one will be able to identify any individuals in the study.

Interventions

BEHAVIORALRelaxation Intervention

Relaxing Music combined with Progressive Muscle relaxation and guided imagery

Sponsors

Towson University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women on bed rest for high risk pregnancy

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
Interview5-7 daysParticipants participated in a follow up interview

Secondary

MeasureTime frameDescription
Post-survey5-7 daysParticipants completed a brief post-survey

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026