TheEffect of a Solution-FocusedApproach on Breastfeeding

Sponsor
Eskisehir Osmangazi University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05663567
Collaborator
(none)
75
1
3
9.5
7.9

Study Details

Study Description

Brief Summary

The Effect of a Solution-FocusedApproach on Breastfeeding Self-efficacy:

A RandomizedControlledStudy It is a single-blind, randomized controlled study with a pre-test post-test design.

In this study, it is aimed to increase the psychosocial health levels of mothers in the postpartum period and to eliminate their concerns about breastfeeding and infant feeding, with a solution-oriented approach planned to be applied to mothers with low breastfeeding self-efficacy. In addition, it is thought that the results of the research will make an important contribution to the national literature.

Question 1: Is a solution-oriented approach effective in increasing mothers' breastfeeding self-efficacy?

Condition or Disease Intervention/Treatment Phase
  • Behavioral: solution oriented approach
N/A

Detailed Description

Solution-Focused Approach (COS) is a therapeutic counseling method developed by Steve de Shazer and Insoo Kim Berg et al. in the mid-1970s. This postmodern approach method focuses on the solution itself rather than going to the root of the problems, revealing the individual's past achievements and positive experiences. aims to remove.

One of the most important advantages of the Solution-Oriented Approach is that it is effective in a short time. Studies have shown that CFS can achieve the desired results between 6 and 10 sessions. It is important that the sessions and techniques of the Solution-Oriented Approach are used in harmony and that the sessions are structured. Particular attention is paid to the first session as it initiates the change and contributes to the process. In Solution-Oriented Approach, sessions are conducted as "first session" and "second and other sessions".

In this study, it is aimed to increase the psychosocial health levels of mothers in the postpartum period and to eliminate their concerns about breastfeeding and infant feeding, with a solution-oriented approach planned to be applied to mothers with low breastfeeding self-efficacy. In addition, it is thought that the results of the research will make an important contribution to the national literature

Study Design

Study Type:
Interventional
Anticipated Enrollment :
75 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Supportive Care
Official Title:
TheEffect of a Solution-FocusedApproach on Breastfeeding Self-efficacy: A RandomizedControlledStudy
Actual Study Start Date :
Oct 26, 2022
Anticipated Primary Completion Date :
Dec 26, 2022
Anticipated Study Completion Date :
Aug 10, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: experimental group 1

Implementing a solution-focused approach to support breastfeeding ONE TO ONE STUDY

Behavioral: solution oriented approach
Implementing a solution-focused approach to support breastfeeding

Experimental: experimental group 2

Implementing a solution-focused approach to support breastfeeding GROUP STUDY

Behavioral: solution oriented approach
Implementing a solution-focused approach to support breastfeeding

No Intervention: No Intervention

ROUTINE MAINTENANCE WILL BE DONE SOLUTION-FOCUSED APPROACH WILL NOT BE APPLIED.

Outcome Measures

Primary Outcome Measures

  1. Increasing mothers' "breastfeeding self-efficacy scale score" [12 weeks]

    increase in breastfeeding success of lactating puerperant women (After the solution-oriented approach application, the breastfeeding self-efficacy scale The Breastfeeding Self-Efficacy Short Form Scale is a 5-point Likert-Type scale with 1= "I am not sure at all" and 5 = "I am always sure". As Bandura (1998) suggested, all items are positive. The minimum score that can be obtained from the scale is 14, and the maximum is 70.

  2. Increasing "Latch breastfeeding scale score" [12 weeks]

    After the solution-oriented approach application, the latch breastfeeding scale will be evaluated. Each item is evaluated between 0-2 points. The total score that can be taken from the scale is 10. The measurement tool has no cut-off point and the higher the LATCH score, the higher the success of breastfeeding.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Over 18 years old, literate,

  • Can speak Turkish,

  • Primiparous and at term and healthy delivery (38-42 weeks, 2500-4000g born, 5th minute APGAR score of 7 and above, no known congenital disease),

  • Women who do not have a chronic disease that prevents breastfeeding in their baby or in themselves

  • Does not have a systemic disease,

  • Those who have never received a planned breastfeeding training before,

  • Having a healthy pregnancy,

  • Planning to breastfeed,

  • Women who have internet access, devices with internet usage (smartphone, computer, tablet, etc.), who have Zoom and Google Meet video conferencing applications on these devices.

  • Women who can be reached within one week at the latest after giving birth

Exclusion Criteria:
  • Women who do not want to breastfeed

  • Women who have a disability to breastfeed

  • Expressing that they cannot continue to work until the end,

  • Women who did not participate and did not answer the post-test of the questionnaires.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Eskisehir Osmnagazi Universty Eskisehir Eskişehir Turkey 26480

Sponsors and Collaborators

  • Eskisehir Osmangazi University

Investigators

  • Principal Investigator: özlem CAGAN, PHD, ocagan@ogu.edu.tr

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
ESRA NUR KABAKCI, RESEARCH ASSİSTMENT, Eskisehir Osmangazi University
ClinicalTrials.gov Identifier:
NCT05663567
Other Study ID Numbers:
  • SFAB
First Posted:
Dec 23, 2022
Last Update Posted:
Dec 27, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Dec 27, 2022