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The effect of mental training in pregnancy in couples and pregnant women on women's mental health

Comparison of the effectiveness and non effectiveness of psycho-educational intervention in couples and pregnant women groups on their mental health in selected health centers of Isfahancity,2015

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016012426174N1
Enrollment
120
Registered
2016-03-15
Start date
2016-03-15
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

Mental health. Mental disorder, not otherwise specified

Interventions

Intervention 1: In the experimental groups at the beginning of the study General Health Questionnaire (GHQ) and depression, anxiety and stress questionnaire ((Dass42) will be provided to participants
Behavior
In the control group at the beginning of the study General Health Questionnaire (GHQ) and depression, anxiety and stress questionnaires ((Dass42) will be provided to participants but will not receive
In the experimental groups at the beginning of the study General Health Questionnaire (GHQ) and depression, anxiety and stress questionnaire ((Dass42) will be provided to participants (group of couple

Sponsors

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

Eligibility

Sex/Gender
All
Age
15 Years to 32 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patient's written consent; Pregnant women with wanted pregnancies and first pregnancy; Singleton pregnancy with gestational age 21 to 25 weeks; No acute obstetric and pregnancy-related problems; Lack of psychological illnesses ; No drug addiction of pregnant woman or her husband ; Lack of serious stress in the past 6 months; No history of infertility and infertility treatment. Exclusion criteria: Disease or particular problem during the study; Preterm delivery; The occurrence of sudden and serious stress before completing a second phase questionnaires like (death of relatives, etc.)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Mental health. Timepoint: Baseline and two weeks after the end of the study (sixth week). Method of measurement: According to the General Health Questionnaire (GHQ).;Depression. Timepoint: Baseline and two weeks after the end of the study (sixth week). Method of measurement: According to depression, anxiety and stress (Dass 42)questionnaire.;Anxiety. Timepoint: Baseline and two weeks after the end of the study (sixth week). Method of measurement: According to depression, anxiety and stress (Dass 42)questionnaire.;Stress. Timepoint: Baseline and two weeks after the end of the study (sixth week). Method of measurement: According to depression, anxiety and stress (Dass 42)questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Akbarian

Esfahan University of Medical Sciences

zahraakbarian2013@gmail.com+98 31337922906

Outcome results

None listed

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