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

The effect of educational intervention based on Ottawa nutritional guidelines on nausea and vomiting and health-related quality of life in women with nausea and vomiting during pregnancy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015011920716N1
Enrollment
60
Registered
2015-04-23
Start date
2015-04-19
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Nausea and vomiting during pregnancy. Excessive vomiting in pregnancy

Interventions

Intervention 1: Intervention group: Training Guide Nutrition Ottawa. Intervention 2: Control group: Routin training for obstetric care.
Prevention
Control group: Routin training for obstetric care
Intervention group: Training Guide Nutrition Ottawa

Sponsors

Mashhad University of Medical Sciences - Deputy of Research and Technology
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

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

Secondary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahbobeh Soltani

Mashhad University of Medical Siences

soltanim912@mums.ac.ir

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026