The Effect of Education Based on Roy Adaptation Model for Infertile Individuals on Adaptation and Coping With Stress

February 3, 2021 updated by: Ayşe Duygu Özbaş, Gaziantep Islam Science and Technology University

Hasan Kalyoncu University Health Sciences Institute

Psychosocial counseling applied together with infertility treatment programs makes infertile women more resistant to stress, increases the effectiveness of infertility treatments and encourages infertile patients to continue treatment by improving their mental health.

It appears that learning adaptation strategies in infertile couples is concurrent with health promotion. In addition to medical treatments, it is aimed to add training to be given in accordance with the Roy Adaptation model, to adapt to the process and infertility, and to control stress in infertile individuals in the management of the process.

The study was planned to examine the effect of education based on the roy adaptation model for infertile individuals on adaptation and coping with stress.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

61

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
      • Gaziantep, Turkey
        • Hasan Kalyoncu Üniversitesi

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 45 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • 18-45age difference

Primary infertility

Exclusion Criteria:

- Secondery infertility

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: receiving health education
Other: Education
Patients will be educated to determine their level of coping with stress and their adaptation.
Experimental: Level of compliance
Other: Education
Patients will be educated to determine their level of coping with stress and their adaptation.
Experimental: Coping with stress
Other: Education
Patients will be educated to determine their level of coping with stress and their adaptation.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Training effectiveness
Time Frame: 3 months
The education given will increase adaptation to infertility and coping with existing stress.
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Gaziantep Islam Science and Technology University

Investigators

  • Principal Investigator: Ayşe Duygu Özbaş, Hasan Kalyoncu University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

March 1, 2021

Primary Completion (Anticipated)

June 1, 2021

Study Completion (Anticipated)

October 1, 2021

Study Registration Dates

First Submitted

January 26, 2021

First Submitted That Met QC Criteria

February 3, 2021

First Posted (Actual)

February 5, 2021

Study Record Updates

Last Update Posted (Actual)

February 5, 2021

Last Update Submitted That Met QC Criteria

February 3, 2021

Last Verified

February 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • Hasan Kalyoncu Unıversity

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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