psychosocial intervention in women with recurrent miscarriage. Recurrent pregnancy loss
Conditions
Interventions
Intervention 1: Intervention group:In the intervention group, content has been prepared for women with frequent abortion experience, which will probably include the implementation of a training progra
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 45 Years
Inclusion criteria
Inclusion criteria: Ability to understand and speak Persian Absence of any physical and mental illness Obtaining a score above 12 based on the Edinburgh Depression Questionnaire Getting a score above 30 based on the Spielberger Anxiety Questionnaire No smoking Recurrent spontaneous abortion as two or three (or more) consecutive abortions The fetus is healthy and single Age 20-45 years Childless or having any number of children before the missed pregnancies Last abortion within the last 1 to 6 months Willingness to participate in research The ability to provide rich and sufficient information on the subject being studied
Exclusion criteria
Exclusion criteria: occurrence of stressful events such as death of relatives, divorce, etc. pregnancy Severe depression and anxiety
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Perceived psycho-social support score. Timepoint: before the start of the intervention and 4 weeks after the start of the intervention. Method of measurement: psychosocial support questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Anxiety score. Timepoint: before the start of the intervention and 4 weeks after the start of the intervention. Method of measurement: Spielberger anxiety questionnaire.;Depression score. Timepoint: before the start of the intervention and 4 weeks after the start of the intervention. Method of measurement: Edinburgh depression questionnaire.;Stress score. Timepoint: before the start of the intervention and 4 weeks after the start of the intervention. Method of measurement: perceived stress questionnaire.;Quality of life score. Timepoint: before the start of the intervention and 4 weeks after the start of the intervention. Method of measurement: 36-question quality of life questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAfsanehtalebi68@gmail.com
Ahvaz University of Medical Sciences
Outcome results
None listed