The effect of Lavender and Dialysis Behavior Therapy on delivery outcomes.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Primiparous Pregnant Women with Insecure Attachment to their Husbands
Exclusion criteria
Exclusion criteria: Literacy Single Pregnancy Voluntary Natural Childbirth and no Medical reason for Cesarean section Lack of high-risk pregnancies such as Heart Disease, Preeclampsia, Diabetes, threat of Preterm Delivery ... Failure to participate in psychological Interventions in the last 6 Months Lack of Experience of Traumatic and Stressful Events in the last 6 Months Do not take Psychological Drugs No Allergies to Lavender and no Olfactory Problems
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pregnancy depression. Timepoint: At the beginning of the Study and 35 Days after the start of the intervention. Method of measurement: Beck Depression Inventory.;Pregnancy anxiety. Timepoint: At the beginning of the Study and 35 Days after the start of the intervention. Method of measurement: Wendenberg Pregnancy Anxiety Questionnaire.;Maternal attachment to the fetus. Timepoint: At the beginning of the Study and 35 Days after the start of the intervention. Method of measurement: Maternal attachment questionnaire to Cranley fetus.;Attachment to spouse. Timepoint: At the beginning of the Study and 35 Days after the start of the intervention. Method of measurement: Attachment Questionnaire to Fraley's wife, Waller and Brennan.;Obvious anxiety score in the Spielberger questionnaire. Timepoint: At the beginning of the study and 35 days after the intervention and during labor and two weeks after delivery. Method of measurement: Spielberger Obvious Anxiety Questionnaire.;Patience score in Khormai, Farmani and Soltani questionnaires. Timepoint: At the beginning of the study and 35 days after the intervention and two weeks after delivery. Method of measurement: Questionnaire of Patience of Date, Command and Soltani.;Fear of childbirth score in Harman questionnaire. Timepoint: At the beginning of the study and 35 days after the start of the intervention. Method of measurement: Harman Maternity Fear Questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of labor pain intensity. Timepoint: Evaluation of labor pain intensity before active phase and in the first and second stage of labor. Method of measurement: McGill Pain Pain Ruler.;Check the duration of labor. Timepoint: The active phase of the first stage of dilatation The duration of labor will be measured twice during 5-7 and 8-10 cm dilatations of the cervix. The second phase of labor is from dilatation of 10 cm of the cervix until the fetus leaves. Method of measurement: Through vaginal examinations.;Postpartum Depression Score from the Edinburgh Questionnaire. Timepoint: Two weeks after delivery. Method of measurement: Edinburgh Postpartum Depression Inventory.;Parental Competency Score from the Wallston-Gibbord Questionnaire. Timepoint: Two weeks after delivery. Method of measurement: Walston-Gibbord Parental Competency Score Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Islamic Azad University