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The Effectiveness of Mindfulness-Based Intervention on Anxiety, Stress and Depression in Perinatal Period

Title of proposal:The Effectiveness of Mindfulness-Based Intervention on Anxiety, Stress and Depression in Perinatal Period: A Randomized Controlled Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110826007418N3
Enrollment
80
Registered
2017-12-29
Start date
2017-08-06
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, depression, anxiety. Mood [affective] disorders

Interventions

Intervention 1: For the intervention group will be provided eight 60-90 minute group sessions second in week. Intervention 2: Control group will recieve the rotine care.
Behavior
For the intervention group will be provided eight 60-90 minute group sessions second in week

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Age between 15 to 45 years First, second and more pregnancy (no history of abortion and stillbirth) Singleton pregnancy and healthy fetus based on ultrasound Gestational age of 26-30 weeks Being literate Willingness to participate in the study and regular attendance to receive the intervention and completion of questionnaires Having a contact number for follow-up

Exclusion criteria

Exclusion criteria: Having history of hospitalization with psychiatric problems Having history of drug abuse; smoking. addiction Experiencing the death of first-degree relatives Experiencing severe stress such as , divorce and other problems in last three months Having complicated pregnancy such as hemorrhage, placenta previa, placenta abrupt ion and ... Having depression score higher than of 20 based on Edinburgh scale Having history of preterm labor MacDonald

Design outcomes

Primary

MeasureTime frame
Anxiety score. Timepoint: Before intervention, 8 weeks after intervention, in active phase labor, 6 weeks post partum. Method of measurement: prinatal anxiety score.;Stress score. Timepoint: Before intervention, 8 weeks after intervention, in active phase labor, 6 weeks post partum. Method of measurement: Percieved Stress Scale.;Depression score. Timepoint: Before intervention, 8 weeks after intervention, in active phase labor, 6 weeks post partum. Method of measurement: Edinburgh Postnatal Depression Scale (EPDS.

Secondary

MeasureTime frame
Cesarean section. Timepoint: After delivery. Method of measurement: Frequency.;Anthropometric indicators of newborn. Timepoint: After delivery. Method of measurement: Centimeter.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactshala barzgar molan

Tabriz University of Medical Sciences

sh.barzgar56@gmail.com+98 41 1479 6969

Outcome results

None listed

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