- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06740695
Health Belief Model Based Education for Pregnant Women With Gestational Diabetes
The Effect of Health Belief Model-Based Education Given to Pregnant Women Via WhatsApp on Self-Efficacy and Risk Perception in Pregnancy in Gestational Diabetes
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: MİNE GÖKDUMAN
- Phone Number: 248 213 82 50
- Email: minegokdumankeles@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Between the ages of 18-35,
- In the second trimester,
- Primiparous,
- Have adequate communication skills,
- Literate,
- Can read and understand Turkish,
- Recently diagnosed with GDM,
- Have a singleton pregnancy,
- Pregnant women who agree to participate in the study will be included.
- Continuing pregnancy school
Exclusion Criteria:
Pregnant women with risky pregnancies,
- Multiple pregnancies were not included in the study.
- Pregnant women with previous type 1 or type 2 diabetes,
- Have a psychiatric diagnosis,
- Have a physical disability,
- Have communication problems will be excluded.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Group
|
|
|
Active Comparator: Education group
|
The training materials were prepared in line with the researchers and expert opinions were obtained. Trainings will be given for two weeks. After the trainings are completed, reminder information will be sent to the pregnant women via text messages every other day to inform them that the trainings are continuing. Reminder information prepared as text messages will be sent to the pregnant women's mobile phones. 4 weeks after the first training, the same training will be reminded again via WhatsApp as a summary training by emphasizing key points. The trainings will be carried out by an expert researcher in the field. In the training content prepared in line with WhatsApp, the risks that may be seen during pregnancy and Gestational Diabetes Mellitus;
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pregnancy Risk Perception Scale (GRP)
Time Frame: 1 HOUR
|
The scale was developed by Heaman and Gupton (2009) to assess the risk perception of pregnant women.
The Turkish validity and reliability study of the scale was conducted by Evcili and Dağlar (2019) .
The risk perception scale consists of 9 items and 2 sub-dimensions.
The scale is a visual analog measurement tool.
The scale consists of 9 items and 2 factors.
There is a 0-100 mm linear line immediately below each item in the scale, indicating "no risk" and "extremely high risk".
The total score of the scale is found by adding the scores for each of the nine items and dividing the obtained score by 9. A score can also be made for the factors of the scale: The score for the "Risk perception of the pregnant woman towards her baby" factor is found by adding the scores for each of the 5 items under this factor and dividing the obtained score by 5.
The score for the "Risk perception of the pregnant woman towards herself" factor is obtained by add
|
1 HOUR
|
|
Self-Efficacy Scale in Gestational Diabetes (GESGD):
Time Frame: 1 HOUR
|
Developed by Polat and Avdal (2020), the Self-Efficacy Scale in Gestational Diabetes is a five-point Likert-type scale consisting of 23 items and four sub-dimensions.
The total Cronbach alpha value of the scale was determined as 0.654.
Its sub-dimensions are Diet and Weight Management, Complication Precautions, Nutrition Education Compliance and Medical Treatment Applications.
It has been emphasized that as the score to be obtained from the scale increases as a result of the coding of the positive and negative expressions in the scale, the individual's self-efficacy will increase and that he/she will be able to effectively perform his/her own care as a result of the training he/she receives.
|
1 HOUR
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024/12 GO 2024/800
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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