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NCT06585111

Effect of Individual Counseling Interventions Based On Health Action Process Approach Model On Breastfeeding Duration

Completed NA Last updated 19 September 2024
What this trial tests

NA trial testing Intervention in Breast Feeding in 68 participants. Completed in 15 September 2023.

Timeline
15 September 2022
Primary endpoint
15 September 2023
15 September 2023

Quick facts

Lead sponsorEge University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment68
Start date15 September 2022
Primary completion15 September 2023
Estimated completion15 September 2023
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Ege University

Who can join

18 and older, female only, with Breast Feeding. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this prospective, randomized controlled experimental clinical trial was to examine the effect of individual counseling interventions based on the Health Action Process Approach Model on breastfeeding duration in twin pregnancies. Women in the intervention group received breastfeeding education using motivational interviewing techniques, while women in the control group received routine clinical education and no intervention. Hypotheses of the study: H1: Women who received individual intervention based on the SESY model have higher prenatal breastfeeding self-efficacy than the control group. H2: Women who received individual intervention based on the SESY model have higher prenatal breastfeeding intentions than the control group. H3: Postnatal breastfeeding self-efficacy of women who received individual intervention based on SESY model is higher than the control group. H4: Breastfeeding motivation of women who received individual intervention based on the SESY model is higher than the control group. H5: Women who received individual intervention based on the SESY model had higher rates of exclusive breastfeeding than the control group. The women in the intervention group were given breastfeeding education with motivational interviewing techniques at 28-38 weeks of pregnancy in the prenatal period and 1-3 days, 1-2 weeks, 4-6 weeks, 4th month and 6th month in the postpartum period. The women in the control group did not receive any training by the researcher.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Intervention

Trials testing the same drug.

Other recruiting trials for Breast Feeding

Currently open trials in the same condition.

Other Ege University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06585111.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing