NCT06209658

Brief Summary

The Teach-Back method was initially developed as a communication technique for patients to remember important information about their diagnosis, treatment or medication and to understand what to do. Method; It requires recalling and explaining any information learned during the interaction between the healthcare team and clients. It has been seen that the use of the tell-what-you-learned method can be used effectively in increasing the learning and comprehension level of individuals who lack health knowledge, contributing to positive health behaviors and reducing the return to health institutions, and it has begun to be used in different areas that require patient education. There are no examples of studies in which the tell-what-you-learned method, which has been brought to the agenda and implemented abroad in recent years, is used in our country. The development of breastfeeding self-efficacy is a very challenging process. Postpartum anxiety occurs in women with low breastfeeding self-efficacy perception. Different training methods are used to initiate and maintain breastfeeding. However, there is no generally accepted method that can bridge the communication gap between patients and healthcare professionals and can be used in health education. It is important to use the tell-what-you-learned method, which is used in patient/client training and is expressed as a communication technique based on expressing what the caregivers have learned in their own words, as it is not enough for the individuals being cared for to say "I understand", in terms of increasing the success of breastfeeding and improving the health of the mother and baby.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 18, 2023

Completed
23 days until next milestone

First Submitted

Initial submission to the registry

November 10, 2023

Completed
2 months until next milestone

First Posted

Study publicly available on registry

January 17, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 20, 2024

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 26, 2024

Completed
Last Updated

September 19, 2024

Status Verified

September 1, 2024

Enrollment Period

5 months

First QC Date

November 10, 2023

Last Update Submit

September 10, 2024

Conditions

Keywords

teach back methodbreastfeeding self-efficacy perceptionanxiety levelprimiparous motherbreastfeeding education

Outcome Measures

Primary Outcomes (2)

  • Collection of post-training data

    Mothers will be given breastfeeding training 3 times using the Teach Back method. First breastfeeding training with teach-back method in the 2nd-5th week after birth. The second breastfeeding training takes place between days 13-17 after birth. Between days 30-42 after birth, the third breastfeeding training takes place. will be given between days. The Breastfeeding Self-Efficacy Scale will be administered after each breastfeeding training. The Breastfeeding Self-Efficacy Short Form Scale is a 5-point Likert-type scale consisting of 14 items (1: not at all confident and 5: always confident). The lowest score that can be obtained from the scale is 14 and the highest score is 70. A high score indicates high breastfeeding self-efficacy.

    two months

  • Collection of post-training data

    The Beck Anxiety Scale will be administered after each breastfeeding education given with the Teach-Back method. The scale, consisting of 21 questions, is a 4-point Likert type. Each item in the scale is scored between 0 (not at all) and 3 (serious). The lowest score that can be obtained from the scale is 0 and the highest score is 63. An increase in the score obtained from the scale indicates that the individual's anxiety increases. A total score from the scale between 8 and 15 indicates mild anxiety, between 16 and 25 indicates moderate anxiety, and between 26 and 63 indicates severe anxiety.

    two months

Secondary Outcomes (2)

  • Collection of post-training data

    two month

  • Collection of post-training data

    two month

Study Arms (2)

experimental group

EXPERIMENTAL

breastfeeding education with Teach Back

Diagnostic Test: breastfeeding education of Teach Back

Control Group

OTHER

breastfeeding education simple explanation

Other: breastfeeding education simple explanation

Interventions

breastfeeding education simple explanation is given and the woman is asked to explain and practice.

experimental group

breastfeeding education simple explanation

Control Group

Eligibility Criteria

Age18 Years - 49 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailsgiving birth for the first time
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Living in Iğdır city center
  • Ability to read and write
  • Don't be primiparous
  • Giving birth at term and in a healthy manner
  • Having a healthy newborn
  • Having had a vaginal or cesarean birth

You may not qualify if:

  • Living in Iğdır city center
  • Ability to read and write
  • Don't be primiparous
  • Giving birth at term and in a healthy manner
  • Having a healthy newborn
  • Having had a vaginal or cesarean birth

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dr. Nevruz Erez State Hospital

Iğdır, 76000, Turkey (Türkiye)

Location

Study Officials

  • gülhan akdemir

    Igdir University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: A total of 70 people, 35 in the experimental group and 35 in the control group, will be included in the study.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
teaching assistant at Igdır University

Study Record Dates

First Submitted

November 10, 2023

First Posted

January 17, 2024

Study Start

October 18, 2023

Primary Completion

March 20, 2024

Study Completion

June 26, 2024

Last Updated

September 19, 2024

Record last verified: 2024-09

Locations