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

P

Pamukkale University

Status

Completed

Conditions

Willing to Have Grandchildren or Having Grandchildren
Not Diagnosed With Any Psychiatric Illness
At Least Primary School Graduate
Voluntarily Accepting to Participate in the Study

Treatments

Behavioral: The training

Study type

Interventional

Funder types

Other

Identifiers

NCT06723184
E-60116787-020-468763

Details and patient eligibility

About

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.

Full description

The research is a randomized controlled experimental study with a pre-test-post-test control group. The research will be conducted with women who are grandmothers. 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. Participants will be reached via social media. In this study, the Introductory Information Form, Pharis Self-Confidence Scale, State-Trait Anxiety Scale and Grandchild Care Knowledge Measurement Questionnaire, which reflect the sociodemographic characteristics of the participants, will be used. Women who apply with the request to receive training will be assigned to the intervention and control groups in a block randomization according to their application numbers. Intention-to-treat analysis will be performed to prevent bias and losses. As the randomization method, "block randomization" will be used to ensure that the sample size is equal in the study and control groups. Randomization will be done using the www.randomizer.org application. Data will be analyzed using the SPSS (23.0) package program. Alpha 0.05 will be accepted for significance. Mann Whitney U test and Chi-Square tests will be used to determine whether there is a difference between the groups in terms of demographic variables. Mann Whitney U test will be used to determine the difference between the Pharis Self-Esteem Scale and State-Trait Anxiety Inventory scale scores between the groups.

Enrollment

48 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Voluntarily accepting to participate in the study
  • At least primary school graduate
  • Willing to have grandchildren or having grandchildren
  • Not diagnosed with any psychiatric illness

Exclusion criteria

  • Not willing to participate in the study
  • Not having at least a primary school degree
  • Being diagnosed with a psychiatric disorder
  • Not having grandchildren or not having grandchildren

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

48 participants in 2 patient groups

Experimental grup
Experimental group
Description:
Experimental grup
Treatment:
Behavioral: The training
Control group
No Intervention group
Description:
No intervention grup

Trial contacts and locations

1

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Central trial contact

Büşra Nur Kutlu, graduate student

Data sourced from clinicaltrials.gov

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