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"The Effec of Consultation Using Positive Approach on Maternal Adaptation and Severity of Pregnancy of Nausea and Vomiting"

The Effec of Consultation Using Positive Approach on Maternal Adaptation and Severity of Pregnancy of Nausea and Vomiting

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150731023423N17
Enrollment
60
Registered
2020-10-31
Start date
2020-11-01
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

Pregnancy Nausea and Vomiting. Mild hyperemesis gravidarum

Interventions

Intervention Group, 6 Sessions Positive Counseling Based on The Protocol of Sligman et al. (2006) will be Received Individually From The 6th Week of Gestation. Each Session will be Done 45 Minutes in

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Having 3-16 Scores Based on RHODES' Pregnancy Nausea and Vomiting Questionnaire Gestational Age 6-10 Weeks Wanted Pregnancy Phone Access Normal Pregnancy The Lack of Chronic Disease The lack of Psychological disease

Exclusion criteria

Exclusion criteria: Having of High-risk Pregnancy Symptoms Occurrence of Severe Stressful Events Such as Divorce or Death of Loved Ones Not Desire to Continue to Participate in The Study More Than Two Absence in Counseling Sessions

Design outcomes

Primary

MeasureTime frame
Severity of Pregnancy Nausea and Vomiting. Timepoint: Before Intervention, Daily up to two Weeks, Immediately After Intervention, and Four Weeks After Intervention. Method of measurement: RHODES' Nausea and Vomiting Severity Questionnaire.;Coping With Pregnancy. Timepoint: Before Intervention, Immediately After Intervention, and Four Weeks After Intervention. Method of measurement: Coping With Pregnancy Questionnaire NuPCI.

Secondary

MeasureTime frame
Severity of Nausea and Vomiting. Timepoint: Before Intervention, The End of The Intervention and 4 Weeks After The Intervention. Method of measurement: Reduz Nausea and Vomiting questionnaire.;Coping with pregnancy. Timepoint: Before Intervention, and 4 weeks after Intervention. Method of measurement: Hamilton coping with pregnancy.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMina Abbasi

Zanjan University of Medical Sciences

mina.abbac@yahoo.com+98 24 3234 5031

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 18, 2026