Health TrialsbyHealthPanel

Esmadem Education Model on High-Risk Pregnant Women

ConditionRisky Pregnancies
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorBurdur Mehmet Akif Ersoy University

About this trial

Pregnancy is a normal and natural process in a woman's life. During this process, anatomical, physiological, biochemical and emotional changes are observed. During pregnancy, sometimes risk situations arise from the mother, sometimes from the fetus. the scope of prenatal care is high today, the main focus is on the physical aspects of care and medical measures. Midwives who provide holistic care should also address spiritual care. Therefore, the esmadem education model will be conducted to examine the effect of the spiritual coping, tolerance and depression of risky pregnancies.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

Having any mental illness

Trial design

Design model

Parallel

Treatments tested in this trial

  • Esmadem Education Model

    Behavioral

    Application Application of the Research The implementation of the research was done in 3 steps. Step 1: In the first stage of the research, after the risky pregnant women who come to the polyclinic are informed about the study, the participants who agree to participate and meet the criteria for inclusion in the research will be determined by randomization. After the pregnant women assigned to the training or control group sign the voluntary consent form and their consent is obtained, Personal InformationForm, Mishel Uncertainty in Illness Scale Depression-Anxiety-Stress Scale Depression-Anxiety-Stress Scale (DASÖ-21) scales will be applied. After the first interviews, the study group will be informed about the sessions and the training will start via zoom. In educational sciences, since the number of groups is between 2-20 people in the acquisition of target behaviors at the conceptual level, two training groups will be created and 15 pregnant women will be in the first group, 15 preg

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: Control GroupNo intervention 0 interventions
Group B: INTERVENTION 1Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Religious Coping Scale

Time frame
aseline and 3 months.
2

Michel Uncertainty Scale in Illness-Community Form,

Time frame
aseline and 3 months.
3

Depression-Anxiety-Stress Scale

Time frame
aseline and 3 months.

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Burdur Mehmet Akif Ersoy University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: