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Guided Imagery on Pregnancy Stress and Sleep Quality in Risky Pregnancy

Effect of Guided Imagery on Pregnancy Stress and Sleep Quality in Risky Pregnancy

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06610513
Enrollment
48
Registered
2024-09-24
Start date
2023-02-01
Completion date
2024-12-31
Last updated
2024-09-24

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

Conditions

Effect of Guided Imagery Application on Pregnancy Stress and Sleep Quality in Risky Pregnant Women Will Be Checked

Keywords

Guided imagery, pregnancy, stress, sleep quality, risky pregnancy

Brief summary

In this thesis study, it is thought that with the guided imagery application to the hospitalized pregnant women, there will be a decrease in their stress levels and an increase in their sleep quality. In our country, there is no study where guided imagery application is used in risky pregnant women. It is thought that new information will be added to the literature as a result of this study. This study will be conducted to determine the effect of guided imagery application on pregnancy stress and sleep quality in risky pregnant women.

Interventions

BEHAVIORALGuided imagery

First meeting: The women will be introduced to the clinic, the purpose of the study will be explained, and a written consent form will be filled out. A Personal Information Form and the Pregnancy Stress Assessment Scale (GSDS-36) and the Richard-Campbell Sleep Scale will be filled out. After the questionnaires are filled out, the vital signs of the pregnant woman will be measured and then a 15-minute guided imagery video will be shown. The vital signs of the patient will be measured again 10 minutes after the guided imagery video is watched.

Sponsors

Cukurova University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

Due to the study's nature, masking could not be performed.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Education level should be primary school or above * Being in the 20th week of pregnancy or above * Being planned to stay in the hospital for at least 5 days * Being hospitalized for the first time during pregnancy * Being within the first 3 days of hospitalization * Knowing and speaking Turkish * Being able to communicate verbally

Exclusion criteria

1. Having had guided imagery before 2. Having a diagnosis of mental illness 3. Having become pregnant through infertility treatment

Design outcomes

Primary

MeasureTime frameDescription
Pregnancy Stress Assessment ScaleDuring 5 days after the first meeting with participantPregnancy Stress Assessment Scale will be implemented to the pregnant women. The degree of anxiety, distress and worry experienced by pregnant women is "definitely not", "mild", "moderate", "serious" or "very serious" and is given on a score ranging from 0 to 4, and the perceived stress levels during pregnancy range from a minimum of 0 to a maximum of 144 points. As the score obtained from the scale increases, it is interpreted that stress increases.

Countries

Turkey (Türkiye)

Outcome results

None listed

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