Investigating the ?Effect of Educational Intervention based on the Ottawa Nutritional guide on Nausea and Vomiting in Pregnant wome

Not Applicable

Recruiting

Conditions: ausea and vomiting of pregnancy.
Nausea and vomiting

Registration Number: IRCT20180218038783N5

Lead Sponsor: Babol University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 60

Inclusion Criteria

The gestational age should be 4-16 weeks (4 full weeks to 15 weeks and 7 days).
Singleton pregnancy.
Mother's age should be 15-45 years.
Be literate in reading and writing.
Not suffering from a known physical or mental illness.
Do not use drugs to reduce nausea and vomiting except vitamin B6.
Score 3-16 in response to the Rhodes questionnaire.
Body mass index is equal to or less than 30.
Do not have hearing, speech or mental retardation.
Do not smoke, use drugs or alcohol.

Exclusion Criteria

Obstetrical problems may occur during the study.
Vomiting that has a cause other than pregnancy.
Being hospitalized due to severe nausea and vomiting of pregnancy.

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Average total score of nausea, vomiting and belching in pregnant women. Timepoint: During the first two weeks from the beginning of the study, all the participants of the intervention and control groups will be given the Rhodes questionnaire to complete, and the intervention group will also be given a checklist for carrying out the Ottawa recommendations. Then, for another two weeks, the intervention and control groups will be given the Rhodes questionnaire and the intervention group will be given the Ottawa educational guide implementation checklist to complete. Pregnant women should complete the Rhodes questionnaire based on their conditions three days before handing it over to the researcher. Method of measurement: Rhodes Nausea and Vomiting Index.

Secondary Outcome Measures

Name	Time	Method
Average sexual satisfaction score. Timepoint: Before the beginning and after the fourth week of the intervention. Method of measurement: Hudson sexual satisfaction questionnaire.