Guided Imagery in Hospitalized Pregnant Women

Not Applicable

Completed

• Conditions: Pregnancy

• Registration Number: NCT06949514
• Lead Sponsor: Menekşe Nazlı AKER

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2025-04-22
• Study First Submitted QC: 2025-04-22
• Study Start: 2025-04-28
• Study First Posted: 2025-04-29
• Primary Completion: 2025-07-28
• Study Completion: 2025-07-28
• Status Verified: 2025-08
• Last Update Submitted: 2025-08-25
• Last Update Posted: 2025-08-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 50

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Change in anxiety	at the beginning of the study, 3 days later	The 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 Depression	at the beginning of the study, 3 days later	The 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 Quality	at the beginning of the study, 3 days later	The 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.

Trial Locations

Locations (1)

Aksaray Eğitim Araştırma Hastanesi; Aksaray, Turkey (Türkiye)