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NCT06723184

Investigation of The Impact of Education Given to Grandmothers on Their Self-Confidence in Baby Care and Anxiety

Completed NA Last updated 12 December 2025
What this trial tests

NA trial testing The training in Voluntarily Accepting to Participate in the Study in 48 participants. Completed in 10 October 2025.

Timeline
13 December 2024
Primary endpoint
10 February 2025
10 October 2025

Quick facts

Lead sponsorPamukkale University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposesupportive care
Enrollment48
Start date13 December 2024
Primary completion10 February 2025
Estimated completion10 October 2025
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Pamukkale University

Who can join

Eligibility, female only, with Voluntarily Accepting to Participate in the Study or At Least Primary School Graduate. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Although there are studies in the literature on the effects of antenatal education on pregnant women, there are no interventional studies on the education of grandmothers, who play an important role in the care of the newborn baby. Therefore, the aim of this study is to examine the effects of antenatal education given to grandmothers on anxiety and self-confidence in baby care. The type of study is a randomized controlled experimental study with pre-post and control groups. The training will be given face to face to grandmothers reached through social media. At the beginning of the study, the sample size was calculated in the G-Power program by taking as reference a similar study in which the same scale (Pharis Self-Confidence Scale) was used. According to the t-test in independent groups, 95% confidence interval, 95% power and high effect size (0.98), a total of 48 people were required, 24 experimental and 24 control. Women who apply to receive training will be assigned to intervention and control groups in a block randomised manner according to their application numbers. Intention-to-treat analysis will be performed to prevent bias and losses. A total of six hours of training will be provided to the intervention group. The program content will be prepared by researchers based on literature and using childbirth preparation education philosophies.

Publications & conference data

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

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Trials by the same sponsor.

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