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NCT06723184
Investigation of The Impact of Education Given to Grandmothers on Their Self-Confidence in Baby Care and Anxiety
NA trial testing The training in Voluntarily Accepting to Participate in the Study in 48 participants. Completed in 10 October 2025.
10 February 2025
Quick facts
| Lead sponsor | Pamukkale University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | supportive care |
| Enrollment | 48 |
| Start date | 13 December 2024 |
| Primary completion | 10 February 2025 |
| Estimated completion | 10 October 2025 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- The training
Conditions studied
- Voluntarily Accepting to Participate in the Study — all drugs for Voluntarily Accepting to Participate in the Study →
- At Least Primary School Graduate — all drugs for At Least Primary School Graduate →
- Willing to Have Grandchildren or Having Grandchildren — all drugs for Willing to Have Grandchildren or Having Grandchildren →
- Not Diagnosed With Any Psychiatric Illness — all drugs for Not Diagnosed With Any Psychiatric Illness →
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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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06723184 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Pamukkale University
- Last refreshed: 12 December 2025
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/NCT06723184.
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