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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02636374
Other study ID # 2015-0105
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 2012
Est. completion date November 2018

Study information

Verified date November 2018
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to examine the effects of a guided imagery intervention on perceived stress in pregnant adolescents.


Description:

Pregnant adolescents attending a local alternative education program will be subjects of this study. Students will participate in four, 15 minute guided imagery sessions over about a 4-6 week period. They will complete a pregnancy specific stress questionnaire before beginning and after completion of the guided imagery protocol. The students will also complete a short 9-question stress measure before and after each of the individual guided imagery sessions.

The specific aims are:

1. to evaluate whether a guided imagery intervention reduces perceived stress in pregnant adolescents; and

2. to evaluate whether a guided imagery intervention enhances well-being in pregnant adolescents.

The hypotheses are that the intervention will reduce perceived stress and enhance well-being in these subjects. The purpose of this study is to assess whether employing a guided imagery intervention with pregnant teens and education will reduce perceived stress levels and improve well-being.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date November 2018
Est. primary completion date November 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 13 Years to 21 Years
Eligibility Inclusion Criteria:

- All pregnant students ages 13-21 enrolled in the alternative education program for parenting teens were eligible to participate

Exclusion Criteria:

- Participants were excluded from the study if they delivered their babies prior to completing four sessions of guided imagery intervention.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Guided Imagery
A fifteen minute recording of gentle music together with soft talking to guide relaxation.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Psychological Stress Measure-9 (PSM-9) score Participants will complete the PSM-9 before and after listening to guided imagery sessions for each of the 4 weekly intervention sessions. The Psychological Stress Measure-9 (PSM-9) is a 9 item questionnaire measuring stress. The original form was published in Canada by Louise Lemyre, PHD and Rejean Tessier, PHD in 1988 and the 9 item was published in 2002. Each response rests on an 8 point likert scale. For general surveys of health and well-being in the workplace, an abridged 9-item version was developed to meet a variety of research needs and applications. The PSM-9 version is used at Hydro-Quebec and Renault (France) as well as in public service, hospitals, community services, and private practice. It has the same psychometric qualities of reliability, validity, and internal consistency (.89) and maintains the same heuristic value for statistics: normality of distribution and responsiveness (Lemyre, Chair, & Lalande-Markon, 2009). 4 weeks
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