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The effect of counseling with spirituality approach on stress and anxiety during pregnancy and delivery

The effect of counseling with spirituality approach on stress and anxiety during pregnancy and delivery: a randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016122710324N37
Enrollment
112
Registered
2017-02-10
Start date
2017-01-27
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress, anxiety and depression during pregnancy and puerperium. mental and behavioural disorders associated with the puerperium

Interventions

The control group will receive routine prenatal cares.
Intervention 1: The control group will receive routine prenatal cares. Intervention 2: For the intervention group will be provided six 60-minute group sessions once a week.
Behavior

Sponsors

Vice chancellor for research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Pregnant women with gestational age of 20 to 24 weeks; Pregnant women with first, second and third pregnancy; Having a contact number for follow-up; Participate in at least 2 sessions of all counseling sessions; Having Edinburgh depression score less than 12 before the intervention; Desire to delivery in Shahid Beheshti hospital of Maraghegh city. Exclusion Criteria: Having a physical diseases (such as epilepsy, heart disease, etc.) according to woman’s expression; Having a mental illness according to woman’s expression; History of hospitalization due to current pregnancy complications (such as preterm labor, placental abruption, Hemorrhage, preeclampsia, etc); History of premature labor and other risk factors for preterm labor; Detection of fetal malformations; Occurrence of recent unpleasant events in the last three months; Using of cigarette, alcohol and opiates and other drugs that affect a person's body and mind; Prior participation in spiritual counseling classes

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Before intervention, 4 weeks after the intervention, during labor and 6 weeks postpartum. Method of measurement: Spielberger State-Trait Anxiety Inventory.;Percieved stress. Timepoint: Before the intervention, 4 weeks after the intervention and during labor. Method of measurement: Perceived Stress Questionnaire.

Secondary

MeasureTime frame
Postpartum depression. Timepoint: 6 weeks postpartum. Method of measurement: Edinburgh Postnatal Depression Scale.;Neonatal anthropometric indices. Timepoint: After childbirth. Method of measurement: Childbirth file.;Delivery type. Timepoint: After childbirth. Method of measurement: Childbirth file.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoomeh Haghighat

Faculty of Nursing & Midwifery, Tabriz University of Medical Sciences

m65haghighat@gmail.com+98 34772699

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026