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Набор скоро начнётся NCT07320079

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

Без фазы С лечением Health Literacy Teach Back

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: teach-back, Control Group.
Кому может быть актуально
Состояния в реестре: Health Literacy, Teach Back. Базовые параметры: 18 лет — 65 лет · Женщины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Turkey (Türkiye)
Следующий шаг
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Официальное название

Evaluation of the Effectiveness of Health Literacy Education Given to Women by Teach-Back Method: Randomized Controlled Trial

Обзор

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.

Подробное описание

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. Women aged between 18 and 65 years with a General Health Questionnaire-12 score below 4 will be included in the study. To determine the participants' socio-demographic and health characteristics, the "Personal Information Form" will be used; to assess general health, the "General Health Questionnaire-12" will be applied; to measure health literacy levels, the "Türkiye Health Literacy Scale-32 (TSOY-32)" will be utilized; and to assess self-efficacy, the "General Self-Efficacy Scale" will be employed. Additionally, the "Training Effectiveness Evaluation Form" will be used to evaluate the effectiveness of the education provided to the experimental group. The study will consist of a total of 74 participants, with 37 in the experimental group and 37 in the control group. Verbal and written consent will be obtained from participants who agree to take part in the study, and the participants will be assigned to groups accordingly. 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 control group will receive standard care.

Вмешательства

  • Другое 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
  • Другое Control Group
    The control group will receive standard care

Первичные конечные точки

  • Health literacy [Срок оценки: Measurements will be taken at baseline, immediately after the training (week 6), and one month after the training (week 10).]
  • The General Self-Efficacy Scale [Срок оценки: Measurements will be taken at baseline, immediately after the training (week 6), and one month after the training (week 10).]

Критерии участия

Критерии включения

  • Women aged between 18 and 65 years
  • Those with a General Health Questionnaire-12 score below 4

Критерии исключения

  • Illiterate women
  • Male individuals
  • Those with communication difficulties
  • Healthcare professionals (physicians, midwives, nurses, etc.)
  • Emergency patients

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Другое

Центры проведения

Turkey (Türkiye) · 1 центр
  • Istanbul University- Cerrahpasa — Istanbul

Идентификаторы

NCT: NCT07320079 · 2025-708

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗