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OpenTrials
Completed

NCT Number: NCT06949514

Guided Imagery in Hospitalized Pregnant Women

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.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Aksaray Eğitim Araştırma Hastanesi

Aksaray, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

guided imagery

Other

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.

Primary outcomes

  1. Change in anxiety

    Time frame: 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.

  2. Change in Depression

    Time frame: 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.

  3. Change in Sleep Quality

    Time frame: 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.

Sponsors and collaborators

Lead sponsor

Menekşe Nazlı AKER

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Apr 29, 2025
Registry last updated
Aug 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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