Trial · NCT07897643
Effects of Nurse-Led Finger Feeding Support on Breastfeeding Self-Efficacy and Early Breastfeeding Outcomes
NCT07897643, Not applicable, Completed, Harran University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effects of Nurse-Led Finger Feeding Support on Breastfeeding Self-Efficacy and Early Breastfeeding Outcomes. Trials, record NCT07897643. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07897643
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effects of Nurse-Led Finger Feeding Support on Breastfeeding Self-Efficacy and Early Breastfeeding Outcomes
- NCT number
- NCT07897643
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 90 participants, actual
- Lead sponsor
- Harran University
- Conditions
- Breastfeeding Self-Efficacy, Breastfeeding Outcomes
- Interventions
- Nurse-Led Finger Feeding Education and Support
- First posted
- 2026-10-27
- Last updated
- 2026-10-27
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Breastfeeding Self-Efficacy Score | Baseline (before intervention), within 24 hours postpartum (after intervention), and 1 month postpartum | Breastfeeding self-efficacy will be assessed using the Breastfeeding Self-Efficacy Scale-Short Form (BSES-SF), consisting of 14 items scored on a five-point Likert scale. Total scores range from 14 to 70, with higher scores indicating greater breastfeeding self-efficacy. Changes in scores over time will be compared between the intervention and control groups. |
| Primary | Change in LATCH Breastfeeding Assessment Score | Baseline (before intervention) and within 24 hours postpartum (after intervention) | Breastfeeding performance will be assessed using the LATCH Breastfeeding Assessment Tool, which evaluates five components: latch, audible swallowing, type of nipple, breast/nipple comfort, and positioning assistance. Each component is scored from 0 to 2, yielding a total score ranging from 0 to 10. Higher scores indicate better breastfeeding performance. Changes in LATCH scores from baseline to before hospital discharge will be compared between the intervention and control groups. |
| Secondary | Exclusive Breastfeeding Status at 1 Month Postpartum | 1 month postpartum | Exclusive breastfeeding status will be assessed through a telephone interview at 1 month postpartum. Mothers will report whether their infants are receiving breast milk only, without formula or other foods or liquids, except medications, vitamins, or oral rehydration solutions. The proportion of infants exclusively breastfed will be compared between groups. |
| Secondary | Formula Feeding Status at 1 Month Postpartum | 1 month postpartum | Formula feeding status will be assessed through a telephone interview at 1 month postpartum. Mothers will report whether their infants are receiving infant formula, either alone or in combination with breast milk. The proportion of infants receiving formula will be compared between groups. |
| Secondary | Breastfeeding Continuation at 1 Month Postpartum | 1 month postpartum | Breastfeeding continuation will be assessed through a telephone interview at 1 month postpartum. Mothers will report whether they are continuing to breastfeed their infants, either exclusively or in combination with formula feeding. The proportion of mothers continuing any breastfeeding will be compared between groups. |
| Secondary | Occurrence of Breastfeeding Problems at 1 Month Postpartum | 1 month postpartum | Breastfeeding problems will be assessed through a telephone interview at 1 month postpartum. Mothers will report whether they have experienced any breastfeeding-related difficulties. The proportion of mothers reporting at least one breastfeeding problem will be compared between the intervention and control groups. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07897643
GET https://conductscience.org/api/trials/v1/NCT07897643/registered