NCT06129292

Brief Summary

This study was planned to determine the effect of the emotional liberation technique on breastfeeding in women experiencing motherhood sadness.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
64

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2024

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

First Submitted

Initial submission to the registry

November 4, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

November 13, 2023

Completed
4 months until next milestone

Study Start

First participant enrolled

March 16, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 23, 2024

Completed
18 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 10, 2024

Completed
Last Updated

August 26, 2024

Status Verified

August 1, 2024

Enrollment Period

4 months

First QC Date

November 4, 2023

Last Update Submit

August 23, 2024

Conditions

Keywords

Emotional Freedom TechniquesBreastfeedingMaternity bluesMidwifery

Outcome Measures

Primary Outcomes (1)

  • The Effect of Emotional Freedom Technique on Breastfeeding in Women Experiencing Maternity Blues

    Emotional Freedom Technique

    Procedure 1: Preliminary tests will be carried out and then the 1st EFT session will be held. 2nd Procedure: After 10 days, the first final tests will be performed and then the second EFT session will be held.

Study Arms (2)

İntervention (EFT) group

EXPERIMENTAL

Personal Information Form, Motherhood Blues Scale and Breastfeeding Self-Efficacy Scale will be applied for pre-test to women who meet our study criteria. To EFT Group; After the first tests are done, the 1st EFT session will be held, the 2nd EFT session will be held 10 days later, and the final tests will be done 10 days later. During this period, affirmations will be given depending on the need. Each session is planned to last an average of 45 minutes - 1 hour, and duration and affirmations will be arranged according to the woman's individual difficulties, perspective, support systems, past traumas and emotional blockages. Procedure 1: Preliminary tests will be carried out and then the 1st EFT session will be held. 2nd Procedure: After 10 days, the first final tests will be performed and then the second EFT session will be held.

Behavioral: EFT group

Control group

NO INTERVENTION

Personal information form, Motherhood Blues Scale and Breastfeeding Self-Efficacy Scale will be applied for pre-test to women who meet our study criteria. After 10 days, the motherhood blues scale and breastfeeding self-efficacy scale will be administered again for the final test.

Interventions

EFT groupBEHAVIORAL

Procedure 1: Preliminary tests will be carried out and then the 1st EFT session will be held. 2nd Procedure: After 10 days, the first final tests will be performed and then the second EFT session will be held.

Also known as: Control Group
İntervention (EFT) group

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsWomen
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Voluntarily agrees to participate in the study,
  • Experiencing motherhood blues
  • Being over 18 years old

You may not qualify if:

  • Leaving the study at any time,
  • Having any obstacle to communication

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Trakya University

Edirne, 22100, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Breast Feeding

Interventions

Control Groups

Condition Hierarchy (Ancestors)

Feeding BehaviorBehavior

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

November 4, 2023

First Posted

November 13, 2023

Study Start

March 16, 2024

Primary Completion

July 23, 2024

Study Completion

August 10, 2024

Last Updated

August 26, 2024

Record last verified: 2024-08

Locations