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Guided Imagery in Hospitalized Pregnant Women

The Effect of Guided Imagery on Anxiety, Depression, and Sleep in Hospitalized Pregnant Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06949514
Enrollment
50
Registered
2025-04-29
Start date
2025-04-28
Completion date
2025-07-28
Last updated
2025-08-29

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

Conditions

Pregnancy

Brief summary

The study will be carried out in two different groups. Participants will be approached after being hospitalized for at least 24 hours. After the pregnant women are evaluated in terms of eligibility criteria for the research, the pregnant women who are eligible will be informed about the research and written informed consent will be obtained from the pregnant women who accept. The random distribution of pregnant women to the study groups will be carried out random.

Interventions

OTHERguided imagery

Participants in this group will receive the guided imagery intervention. They will be approached after being hospitalized for at least 24 hours. The guided imagery audio recording will be played for the pregnant women every evening before sleep for three consecutive days.

Sponsors

Menekşe Nazlı AKER
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Being 18 years of age or older * Having no difficulties in understanding and speaking Turkish * Being hospitalized for at least 24 hours * Being in the second trimester of pregnancy (14-28 weeks) * Having a medically stable condition * Experiencing sleep disturbances * Voluntarily agreeing to take part in the study

Exclusion criteria

* Having a hearing impairment * Having ongoing severe vaginal bleeding * Having a diagnosed psychiatric disorder and/or using psychiatric medication * Having uncontrolled hypertension * Presence of intrauterine fetal demise * Premature rupture of membranes (PROM) * Being in preterm labor

Design outcomes

Primary

MeasureTime frameDescription
Change in anxietyat the beginning of the study, 3 days laterThe Hospital Anxiety and Depression Scale is a four-point Likert-type scale used to determine the risk, level, and change in severity of anxiety and depression in patients. The scale consists of 14 items; odd-numbered items assess anxiety, and even-numbered items assess depression. For the anxiety subscale, the cut-off score is 10/11. Individuals scoring above this threshold are considered to be at risk. The lowest possible score on the scale is 0, and the highest possible score is 21.
Change in Depressionat the beginning of the study, 3 days laterThe Hospital Anxiety and Depression Scale is a four-point Likert-type scale used to determine the risk, level, and change in severity of anxiety and depression in patients. The scale consists of 14 items; odd-numbered items assess anxiety, and even-numbered items assess depression. For the depression subscale, the cut-off score is 7/8. Individuals scoring above this threshold are considered to be at risk. The lowest possible score on the scale is 0, and the highest possible score is 21.
Change in Sleep Qualityat the beginning of the study, 3 days laterThe Richard-Campbell Sleep Questionnaire consists of six items that evaluate the depth of night sleep, time taken to fall asleep, frequency of awakenings, duration of wakefulness upon awakening, overall sleep quality, and the level of noise in the environment. Each item is assessed using a visual analog scale ranging from 0 to 100. Scores between 0-25 indicate very poor sleep, while scores between 76-100 indicate very good sleep. As the total score increases, the sleep quality of patients also improves.

Countries

Turkey (Türkiye)

Outcome results

None listed

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