Actively Recruiting

Phase Not Applicable
Age: 19Years - 35Years
FEMALE
Healthy Volunteers
NCT07058766

Development of Post-Disaster Care Protocol for Pregnant Women and Evaluation of Its Effectiveness

Led by Sakarya University · Updated on 2025-07-10

43

Participants Needed

1

Research Sites

53 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

It was designed as a randomized controlled experimental study to determine whether the care protocol planned for pregnant women in the disaster area positively affects their physical and psychological health.

CONDITIONS

Official Title

Development of Post-Disaster Care Protocol for Pregnant Women and Evaluation of Its Effectiveness

Who Can Participate

Age: 19Years - 35Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Over the age of 18
  • Positive (+) pregnancy
  • Able to read and write Turkish and speak and understand Turkish
  • No mental or psychological disorder that would cause difficulty in expressing oneself
  • Not receiving a score between 20-27 (severe depression) on HSA-9
  • No chronic disease or high-risk pregnancy diagnosis requiring hospitalization and follow-up
  • Volunteer to participate in the study
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Foreign nationals who cannot read or write Turkish and are inadequate in speaking or understanding Turkish
  • Those with any mental or psychological disorder/diagnosis
  • Those who score between 20-27 (severe depression) on HSA-9
  • Those with a chronic disease or a diagnosis of high-risk pregnancy requiring hospitalization and follow-up
  • Those who do not agree to participate in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hatay Mustafa Kemal Üniversitesi

Hatay, Turkey (Türkiye)

Actively Recruiting

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Research Team

D

Döndü SEVİMLİ GÜLER, Dr. Lecturer

CONTACT

H

Hatice Tambağ, Prof. Dr.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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Development of Post-Disaster Care Protocol for Pregnant Women and Evaluation of Its Effectiveness | DecenTrialz