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Online Education and Counseling Regarding Gynecological Examination

A

Aydin Adnan Menderes University

Status

Completed

Conditions

Gynecological Disease

Treatments

Behavioral: Online education and counseling

Study type

Interventional

Funder types

Other

Identifiers

NCT05687227
BELMA TOPTAŞ ACAR

Details and patient eligibility

About

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.

Full 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.

Enrollment

100 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups

EXPERIMENT GROUP
Experimental group
Description:
The trainings were held in groups of 4-6 people. The trainings, which were held in three sessions, were held on the days and times that were convenient for the participants. Since the participants were required to attend all sessions, additional session/sessions were held in case of not being able to attend the trainings. Participants in the control and experimental groups were called and the day they would come for the control was determined, and they went to the gynecology outpatient clinic. The post-test questionnaire was applied to the participants in the control and experimental groups in the first 3 months. Until the end of the research, the participants were told that they could reach the researcher at any time and ask questions. Finally, at the 6th month, a post-test form was applied to the participants.
Treatment:
Behavioral: Online education and counseling
CONTROL GROUP
No Intervention group
Description:
No training or counseling was given to the control group. Participants in the control and experimental groups were called and the day they would come for the control was determined, and they went to the gynecology outpatient clinic. The post-test questionnaire was applied to the participants in the control and experimental groups in the first 3 months. Finally, at the 6th month, a post-test form was applied to the participants.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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