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The effect of logo therapy on anxiety and coping with unplanned pregnancy: a randomized controlled trial

The effect of logo therapy on anxiety and coping with unplanned pregnancy: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231107059988N1
Enrollment
52
Registered
2023-11-25
Start date
2023-11-22
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Unplanned pregnancy.

Interventions

Intervention 1: Intervention group: the intervention group (26 women), meetings will be held in groups of 3-5 people once a week for consecutive weeks. The place of consultation will be the nearest he

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 49 Years

Inclusion criteria

Inclusion criteria: Married women aged 18-49 years Women with an unplanned pregnancy with a decision to continue the pregnancy with a gestational age of 16 to 24 weeks Ability to communicate Women whose anxiety score is between 8-19 (mild, moderate, severe anxiety) in the DASS-21 questionnaire

Exclusion criteria

Exclusion criteria: Cases of fetal abnormalities Having a high-risk pregnancy including diabetes, high blood pressure, chronic diseases affecting pregnancy such as heart disease, vascular disease, lung disease, etc. History or current suffering from mental problems or history of hospitalization in a psychiatric hospital (according to the individual's own statement) Experiencing an unfortunate incident in the last six months, including the death of a loved one

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: At the beginning of the study and 4 weeks after the end of the intervention. Method of measurement: DASS-21 questionnaire.;Coping. Timepoint: At the beginning of the study and 4 weeks after the end of the intervention. Method of measurement: Revised pregnancy coping inventory: NU-PCI.

Secondary

MeasureTime frame
Health practice. Timepoint: At the beginning of the study and 4 weeks after the end of the intervention. Method of measurement: Health Practices Questionnaire-II: HPQ-II.;Quality of life in pregnancy. Timepoint: At the beginning of the study and 4 weeks after the end of the intervention. Method of measurement: QOL-GRAV: Quality of life-Gravity.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Yavari kia

Tabriz University of Medical Sciences

p_k_hn@yahoo.com+98 41 3479 6770

Outcome results

None listed

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