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Examining the Effectiveness of solution-focused brief consolation on mothers with gestational diabetes under insulin treatment

Examining the Effectiveness of solution-focused brief consulation with emphasis on self-efficacy on stress and depression and anexity of mothers with gestational diabetes under insulin treatment

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200202046339N1
Enrollment
56
Registered
2020-02-17
Start date
2019-10-23
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

stress,anexity,depression, in mothers with gdm. Gestational diabetes mellitus in pregnancy

Interventions

Intervention 1: Intervention group: prenatal care + intervention ,Intervention consist of 6session: In the first session, introduction, After that, mothers were provided with the content of Principles

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Mothers at10-38 week gestational age Mothers Have at least a fifth grade(primary) education non-smoking and no addiction to psychological drug or alcohol,... no history of medical illnesses, such as, cardiovascular diseases, hypertension, epilepsy, migraine, thyroid disease, connective tissue disease, asthma, respiratory disorders, kidney failure, anemia, and stroke, no histotry of hospitalization due to mental illnesses or abuse of psychological drugs under insulin treatment singleton pregnancy

Exclusion criteria

Exclusion criteria: individuals who were unwilling to continue the research absent more than one session, of 6 consultation sessions. who experienced pregnancy-related complications, including bleeding, hypertension, early delivery, and surgery or hospitalization for current pregnancy, as well as delivery or abortion during the study severe psychiatric disorders or disaster, happened in pregnancy occurrence of major stressful events during the study

Design outcomes

Primary

MeasureTime frame
Stress score in dass21 scale. Timepoint: Before intervention, 6 week and 16 week after intervention. Method of measurement: dass21 scale.;Anexity score in dass21 scale. Timepoint: Before intervention,6 week and 16 week after intervention. Method of measurement: dass21 scale.;Depression score in dass21 scale. Timepoint: Before intervention,6 week and 16 week after intervention. Method of measurement: dass21 scale.;Behavioral sterategies for coping with steress. Timepoint: Before intervention,6 week and 16 week after intervention. Method of measurement: ciss scale.

Secondary

MeasureTime frame
Self efficacy. Timepoint: Before intervention,6 week ,16 week after intervention. Method of measurement: Dmses scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRafiee Zahra

Arak University of Medical Sciences

Zrfyy475@gmail.com+98 25 3289 6264

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 24, 2026