CClinicalTrials.gg
Status unknownNCT04929561Updated Jun 18, 2021

The Effect of Breastfeeding Support Provided Via Video-conferencing

An interventional study of Video-conferencing group in Breastfeeding, Anxiety Disorders and Neonatal Outcomes, sponsored by Kahramanmaras Sutcu Imam University. Status unknown at 1 site in Turkey. Open to participants aged 19 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-06-18.

Sponsored by Kahramanmaras Sutcu Imam University · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Jun 2021), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 9 months after the study started (first participant enrolled Aug 2020, registered Jun 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
78
Allocation
Randomized
Ages
19 Years and older
Sex
All
01

Study summary

A randomized control trial was made to examine the effects of breastfeeding support given by the video-conferencing method in the early postpartum period on anxiety, breastfeeding self-efficiency, and newborn outcomes.

02

Conditions studied

  • Breastfeeding
  • Anxiety Disorders
  • Neonatal Outcomes

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03

In context

Anxiety Disorders

4,868 studies on the registry are indexed under Anxiety Disorders; 1,390 are open to participants now.

This study's planned enrollment of 78 is close to the median of 80 across 4,174 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

Kahramanmaras Sutcu Imam University is the lead sponsor of 192 studies on the registry; 40 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

Infants;

  • Born between 37 and 42 weeks
  • Without severe congenital anomalies

Mothers;

  • A single live birth
  • Were 18 years of age or over
  • At least primary school graduate
  • Did not have a disease that prevents breastfeeding
  • Had internet access at home or on the phone
  • Could speak and understand the Turkish language.

Exclusion criteria

Exclusion Criteria:

  • Situations that cause separation of mother and baby
  • Hospitalization of the baby in intensive care
  • Inability to answer 3 calls in a video call
  • They were determined as those who could not be reached during the home visit for the first and second follow
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
78 participants (estimated)

Study arms

  • Experimental
    Video-conferencing group

    The mothers in the video-conferencing group were counseled via video-conferencing a total of six times (three times a week, at equal intervals) during the first 2 weeks after birth. Each interview was approximately 15-20 minutes. In video-conferencing sessions, the breastfeeding position, the mother's grasping the breast, the baby's latch-on, and sucking duration were observed. Mothers' questions were answered and solutions were offered for breastfeeding problems (sore nipple, engorgement, etc.).

    Behavioral: Video-conferencing group

  • No intervention
    Control group

    The mothers in the control group were given usual care before discharge and no intervention was made after discharge.

Interventions

  • BehavioralVideo-conferencing group

    No intervention

    Also known as: Control group

06

What researchers measure

Primary outcomes

  1. The mean postpartum maternal anxiety level (mean ± SD)

    The primary outcome of this study was the mean postpartum maternal anxiety level (mean ± SD) of the mothers at 2 weeks and 4 weeks after delivery. Maternal anxiety level was assessed using the Postpartum Specific Anxiety Scale. The scale comprises 51 items and 4 sub-dimensions. It means that those who score 73 and below on the scale have low postpartum anxiety levels, those who score between 74 and 100 have a medium level, and those who score 101 and above have a high level of anxiety.

    Time frame: at 2 weeks and 4 weeks after delivery

  2. The mean breastfeeding self-efficacy level

    The other main outcome of the study was the mean breastfeeding self-efficacy level (mean ± SD) measured with the Breastfeeding Self-Efficacy Scale Short Form. The scale is likert type and a total score between 14 and 70 is taken from the scale. The higher the score, the higher the breastfeeding self-efficacy.

    Time frame: at 2 weeks and 4 weeks after delivery

Secondary outcomes

  1. Neonatal outcomes-Newborn weight (g)

    Newborn weight (g) was evaluated using the Follow-up Form at 2 weeks and 4 weeks after delivery

    Time frame: at 2 weeks and 4 weeks after delivery

  2. Neonatal outcomes-Hypoglycemia of the newborn

    Hypoglycemia of the newborn was evaluated using the Follow-up Form at 2 weeks and 4 weeks after delivery.

    Time frame: at 2 weeks and 4 weeks after delivery

  3. Neonatal outcomes-Need for phototherapy

    The need for phototherapy was evaluated using the Follow-up Form at 2 weeks and 4 weeks after delivery

    Time frame: at 2 weeks and 4 weeks after delivery

  4. Neonatal outcomes-Respiratory morbidity

    Respiratory morbidity was evaluated using the Follow-up Form at 2 weeks and 4 weeks after delivery

    Time frame: at 2 weeks and 4 weeks after delivery

  5. Neonatal outcomes-illness requiring hospitalization

    Illness requiring hospitalization was evaluated using the Follow-up Form at 2 weeks and 4 weeks after delivery

    Time frame: at 2 weeks and 4 weeks after delivery

  6. Neonatal outcomes-Food intake other than breast milk

    Food intake other than breast milk was evaluated using the Follow-up Form at 2 weeks and 4 weeks after delivery

    Time frame: at 2 weeks and 4 weeks after delivery

  7. Neonatal outcomes-Neonatal death

    Neonatal death was evaluated using the Follow-up Form at 2 weeks and 4 weeks after delivery

    Time frame: at 2 weeks and 4 weeks after delivery

07

Study locations

1 of 1 sites recruiting
  • Kahramanmaras Sutcu Imam University
    Kahramanmaras, Kahramanmaraş 4600, Turkey
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 18, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04929561
Lead sponsor
Kahramanmaras Sutcu Imam University
Responsible party
Deniz Akyıldız (Assistant Professor, Kahramanmaras Sutcu Imam University) — Principal investigator
First posted
Jun 18, 2021
Start date
Aug 25, 2020
Primary completion
Sep 30, 2021 (estimated)
Completion
Sep 30, 2021 (estimated)
Last update
Jun 18, 2021

Study contacts

Deniz Akyıldız, PhD
Contact
denizbtm@gmail.com
05069851358
Deniz Akyıldız
Contact
denizbtm@gmail.com
05069851358
Betül Bay
principal investigator · Kahramanmaras Sutcu Imam University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2021. You cannot join it, but the record below documents what was studied.

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