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

Phase 3
Recruiting
Conditions
Mild hyperemesis gravidarum
Pregnancy Nausea and Vomiting.
O21.0
Registration Number
IRCT20150731023423N17
Lead Sponsor
Zanjan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
60
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

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

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
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.
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