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Clinical Trials/NCT05687227
NCT05687227
Completed
Not Applicable

The Effect on Women's Attitude and Anxiety Levels Regarding Gynecological Examination of Online Education and Counseling

Aydin Adnan Menderes University1 site in 1 country100 target enrollmentJune 4, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gynecological Disease
Sponsor
Aydin Adnan Menderes University
Enrollment
100
Locations
1
Primary Endpoint
A pre-test was applied to 100 women constituting the sample of the study.
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This research was carried out to determine the effect of online education and counseling on women's attitudes and anxiety levels regarding gynecological examination.

The research is a pre-test-post-test, randomized controlled experimental study.

Detailed Description

The research is a pre-test-post-test, randomized controlled experimental study. Simple randomization method was used to assign the participants to the groups. The sample consisted of a total of 100 women (experimental group: 50 women and control group: 50 women). The study was carried out with women who applied to Aydın Adnan Menderes University Application and Research Hospital, Gynecology Clinic, Gynecology Outpatient Clinic and met the study criteria.

Registry
clinicaltrials.gov
Start Date
June 4, 2021
End Date
September 7, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Aydin Adnan Menderes University
Responsible Party
Principal Investigator
Principal Investigator

Belma Toptas Acar

Principal Investigator

Aydin Adnan Menderes University

Eligibility Criteria

Inclusion Criteria

  • Applying to Aydın Adnan Menderes University Application and Research Hospital, Gynecology Clinic, Gynecology Clinic,
  • Coming to the examination within the first 3 months after the examination,
  • Internet access,
  • Having a Whatsapp or e-mail address,
  • Able to read and write,
  • Able to speak and understand Turkish,
  • Women in the 18-50 age group are included.

Exclusion Criteria

  • Having a communication (speech, hearing, etc.) disability,
  • Having any psychological illness,
  • Pregnant and postpartum,
  • Diagnosed with cancer,
  • Women who received infertility diagnosis and treatment were excluded.

Outcomes

Primary Outcomes

A pre-test was applied to 100 women constituting the sample of the study.

Time Frame: up to 9 months.

Before the online training and counseling, a pre-test was applied to a total of 100 participants, 50 of which were in the experimental group and 50 in the control group. In the pre-test question form created by the researcher in the light of the literature, sociodemographic (questions 1-9), obstetrics (questions 10-13), gynecological characteristics (questions 14-23) and attitudes towards gynecological examination (16 questions ).

The State and Trait Anxiety Inventory was applied to 100 women constituting the sample of the study.

Time Frame: up to 9 months.

The State and Trait Anxiety Inventory, which was developed by Spielberger (1970) and adapted to Turkish by Öner and Le Compte in 1983, was used. The first 20 questions in the scale measure "state anxiety" and the next 20 questions measure "trait anxiety". A score of 0-19 indicates no anxiety. While 20-39 indicates mild anxiety, 40-59 moderate and 60-79 severe anxiety, 80 points are considered as panic. The minimum value to be taken from the state anxiety scale is "0" and the maximum value is "80". The minimum value to be taken from the trait anxiety scale is "0" and the maximum value is "80". As the score increases, the level of anxiety also increases.

Secondary Outcomes

  • The State and Trait Anxiety Inventory was applied to 68 people who were pretested within the first 3 months after the pretest was applied.(The pre-test implementation phase was completed in 9 months. This process took a total of 1 year, since the last test was applied to the last participants within the 3rd month.)
  • The posttest was applied to 68 people who were pretested within the first 3 months after the pretest was applied.(The pre-test implementation phase was completed in 9 months. This process took a total of 1 year, since the last test was applied to the last participants within the 3rd month.)

Study Sites (1)

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