The effect of educational intervention based on Ottawa nutritional guidelines on nausea and vomiting and health-related quality of life in wome

Not Applicable

• Conditions: ausea and vomiting during pregnancy.; Excessive vomiting in pregnancy

• Registration Number: IRCT2015011920716N1
• Lead Sponsor: Mashhad University of Medical Sciences - Deputy of Research and Technology

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

1) Signing informed consent and being Iranian and resident of Mashhad.
2) The phone number available for contact.
3) Gestational age 11-6 Week (6 weeks and 1 day to 10 weeks and 6 days) .
4) Singleton pregnancy.
5) Age 18- 35 years old.
6) have a minimum education.
7) No physically and mentally ill.
8) Not using herbal remedies to reduce nausea and vomiting.
9) In response to the tool Rhodes score of 3 to 16 win.
10) BMI is equal to or less than 30.
11) Pregnancy is required.
12) No pregnancy following assisted reproductive techniques.
13) No audio problem and no mental retardation.
14) No history of two consecutive miscarriages before pregnancy.
15) No smoking, no drugs and alcohol.
16) The history of stressful events during the last six months is not.
17) 21-DOS in response to the questionnaire score less than 10, 14, 17, respectively, in the areas of depression, anxiety and stress attend..
Exclusion criteria:
1) No tendency to continue to participate in the study.
2) Obstetric complications occurred during the study.
3) vomit that is a cause other than pregnancy.
4) Admission due to severe nausea and vomiting of pregnancy.
5) Not attending in one of the sessions

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ausea and vomiting pregnancy. Timepoint: Four weeks after the intervention with two-week intervals. Method of measurement: Index of Nausea and vomiting Rhodes.

Secondary Outcome Measures

Name	Time	Method
Health-related quality of life after 4 weeks of study. Timepoint: The second week until the fourth week intervals for three days. Method of measurement: Health-Related Quality of Life Questionnaire in women with nausea and vomiting of pregnancy.