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Clinical Trials in Turkey / NCT07320079
Recruiting Not applicable

Evaluation of the Effectiveness of Health Literacy Education Given to Women by Teach-Back Method

NCT07320079 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-02
Last updated
2026-08-14

Condition(s) studied

Health LiteracyTeach Back

Investigational drug(s) / intervention(s)

teach-backControl Group

teach-back: The experimental group will receive face-to-face health literacy education using the teach-back method in six sessions, each lasting 45 minutes per week. The training will be provided by the researcher on a one-to-one basis. Health literacy education will be delivered using the teach-back method. After each session, participants will be asked to repeat what they have learned in their own words. The researcher will assess how well the participants have understood the topic. Any misunderstandings will be identified and corrected. During this process, participants will also have the opportunity to ask questions. Additional information will be provided if necessary until participants can accurately repeat the expected knowledge. The module will be considered complete once the participants have correctly expressed the information and understood the topic. The following week, the next module will begin, and this process will continue until all six modules are completed.

Control Group: The control group will receive standard care

Study summary

This study aims to enhance women's health literacy levels and to examine the effectiveness of the teach-back teaching technique in improving women's health literacy. The research was designed as a randomized controlled study. In addition, this study aims to answer the question of whether health literacy education delivered using the teach-back method is effective in improving women's health literacy levels. Within the scope of the study, participants in the experimental group will receive health literacy education using the teach-back technique, while the control group will receive standard care. Data will be collected using a questionnaire method.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Women aged between 18 and 65 years * Those with a General Health Questionnaire-12 score below 4 Exclusion Criteria: * Illiterate women * Male individuals * Those with communication difficulties * Healthcare professionals (physicians, midwives, nurses, etc.) * Emergency patients

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Istanbul University- Cerrahpasa Istanbul Turkey (Türkiye) Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07320079 on ClinicalTrials.gov ↗ ← All trials in Turkey