Skip to main content
Clinical Trials/NCT07407322
NCT07407322
Completed
Not Applicable

Effect of Affirmation-Based Information on Stress and Intolerance of Uncertainty in High-Risk Pregnant Women Admitted to the Emergency Department: A Randomized Controlled Trial

Nilgun Avci1 site in 1 country102 target enrollmentStarted: July 1, 2024Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Nilgun Avci
Enrollment
102
Locations
1
Primary Endpoint
Perceived Stress Level

Overview

Brief Summary

This study examined whether providing affirmation-based information to high-risk pregnant women admitted to the obstetrics emergency department could reduce stress levels and intolerance of uncertainty. High-risk pregnancy can be emotionally challenging, especially in emergency settings, and supportive communication may help women cope with stress during this period.

In this randomized controlled trial, pregnant women diagnosed with high-risk pregnancy were assigned either to an intervention group that received routine emergency care along with verbal information and positive affirmation statements, or to a control group that received routine emergency care and verbal information only. Stress levels and intolerance of uncertainty were measured before and after the intervention using validated assessment tools.

The findings of this study aim to contribute to evidence-based supportive care practices in obstetric emergency settings and to inform health care professionals about non-pharmacological approaches to improving emotional well-being in high-risk pregnant women.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Women aged 18 years and older
  • Gestational age of 32 weeks or above
  • Diagnosed with high-risk pregnancy
  • Admitted to the obstetrics emergency department
  • Volunteered to participate and provided written informed consent

Exclusion Criteria

  • Inability to communicate in Turkish
  • No diagnosis of high-risk pregnancy

Arms & Interventions

Affirmation-Based Information

Experimental

Pregnant women received routine emergency obstetric care, structured verbal information about the emergency unit and their current condition, followed by affirmation statements delivered verbally in a calm and supportive tone during non-stress test monitoring.

Intervention: Affirmation + Information Group (Behavioral)

Control group

No Intervention

Pregnant women received routine emergency obstetric care and structured verbal information about the emergency unit and their current condition during non-stress test monitoring.

Outcomes

Primary Outcomes

Perceived Stress Level

Time Frame: Baseline and immediately after the intervention during emergency department observation

Change in perceived stress measured by the Neuman Systems Model-Based Perceived Stress Scale for High-Risk Pregnancy.

Secondary Outcomes

  • Intolerance of Uncertainty(Baseline and immediately after the intervention)

Investigators

Sponsor
Nilgun Avci
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Nilgun Avci

phD

Biruni University

Study Sites (1)

Loading locations...

Similar Trials