Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
50 participants
INTERVENTIONAL
2025-04-28
2025-07-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
DOUBLE
Study Groups
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Intervention Group
Guided imagery group
guided 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.
Control Group
Control Group
No interventions assigned to this group
Interventions
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guided 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.
Eligibility Criteria
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Inclusion Criteria
* 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 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
18 Years
FEMALE
No
Sponsors
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Menekşe Nazlı AKER
OTHER
Responsible Party
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Menekşe Nazlı AKER
Assist. Prof.
Principal Investigators
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Menekşe Nazlı Aker
Role: STUDY_DIRECTOR
Assistant professor
Locations
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Aksaray Eğitim Araştırma Hastanesi
Aksaray, , Turkey (Türkiye)
Countries
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Other Identifiers
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06.01.2025/01-14
Identifier Type: -
Identifier Source: org_study_id
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