Skip to main content
OpenTrials
Completed

NCT Number: NCT07544095

Guided Imagery for Nausea and Well-Being in Pregnant Women

This study aims to evaluate the effect of a guided imagery-based psychoeducational intervention on nausea and vomiting severity and psychological well-being in pregnant women. The intervention includes structured psychoeducation and guided imagery sessions designed to promote relaxation, enhance symptom management, and improve overall well-being. Pregnant women in the first trimester experiencing nausea and vomiting were randomly assigned to either the intervention group or the control group. The intervention group received a four-session guided imagery-based psychoeducation program supported by home-based audio practice, while the control group received routine antenatal care. Outcomes were assessed before and after the intervention using standardized measurement tools.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Primary Health Care Center

Muş, Turkey (Türkiye)

About this study

This randomized controlled study was conducted to determine the effect of a guided imagery-based psychoeducational intervention on nausea and vomiting severity and psychological well-being in pregnant women. The study included pregnant women in their first trimester who were experiencing nausea and vomiting and met the inclusion criteria.

Participants were randomly assigned to either the intervention group or the control group. The intervention group received a structured psychoeducational program based on guided imagery techniques. The program consisted of four face-to-face sessions, each lasting approximately 20-25 minutes. The first session included information about the relationship between nausea, vomiting, and psychological processes, as well as an introduction to guided imagery. Participants were also provided with an audio recording to support daily home practice. In subsequent sessions, guided imagery techniques were applied to reduce nausea symptoms, enhance relaxation, and promote psychological well-being. Participants were encouraged to practice the technique regularly and especially during episodes of nausea.

The control group received routine antenatal care without any additional intervention. Data were collected from both groups before and after the intervention using standardized instruments, including the Pregnancy Unique Quantification of Emesis (PUQE) scale and a psychological well-being scale.

The study was retrospectively registered. Ethical approval was obtained from the Inonu University Health Sciences Scientific Research Ethics Committee (Approval No: 2024/5747).

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Being 18 years of age or older
  • Being in the first trimester of pregnancy (≤14 weeks)
  • Experiencing nausea and vomiting during pregnancy
  • Having a singleton pregnancy
  • Being able to read and understand Turkish
  • Voluntarily agreeing to participate in the study

Exclusion criteria

  • Having a high-risk pregnancy (e.g., preeclampsia, gestational diabetes, placenta previa)
  • Diagnosis of hyperemesis gravidarum
  • Having a diagnosed psychiatric disorder or receiving psychiatric treatment
  • Having a condition that may prevent participation in guided imagery (e.g., hearing or cognitive impairment)
  • Previous experience with guided imagery or similar psychological interventions

Treatment and study plan

Guided Imagery-Based Psychoeducation

Behavioral

A structured psychoeducational program based on guided imagery techniques, consisting of four face-to-face sessions aimed at reducing nausea and vomiting symptoms and improving psychological well-being. Participants were instructed to practice guided imagery daily at home using standardized audio recordings.

Primary outcomes

  1. Nausea and Vomiting Severity

    Time frame: Baseline and after completion of the 4-session intervention (approximately 2 weeks)

    Nausea and vomiting severity will be assessed using the Pregnancy Unique Quantification of Emesis (PUQE) scale. Higher scores indicate greater severity of symptoms.

Secondary outcomes

  1. Psychological Well-Being

    Time frame: Baseline and after completion of the intervention (approximately 2 weeks)

    Psychological well-being will be evaluated using a standardized psychological well-being scale. Higher scores indicate better psychological well-being.

Sponsors and collaborators

Lead sponsor

Inonu University

Other

Registry information

Official study title

The Effect of a Guided Imagery-Based Psychoeducational Intervention on Nausea, Vomiting, and Psychological Well-Being in Pregnant Women: A Randomized Controlled Trial

Acronym: GI-PREG

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Apr 22, 2026
Registry last updated
Apr 22, 2026

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.

Published trials that share one or more normalized conditions with this study.