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

Investigating the effect of Educational Intervention based on the Ottawa Nutritional guide on Nausea and Vomiting in Pregnant women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180218038783N5
Enrollment
60
Registered
2023-09-03
Start date
2023-11-01
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Nausea and vomiting of pregnancy. Nausea and vomiting

Interventions

Intervention 1: Intervention group: After people are placed in two intervention and control groups, two days a week will be determined for pregnant women in the intervention group, one day before the
other recommendations on lifestyle and acupressure) with lecture methods, question and answer and group discussion, lecture with slide show will provide. The educational content will include: the firs

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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

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

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Fereshteh Behmanesh

Babol University of Medical Sciences

f.behmanesh@mubabol.ac.ir+98 11 3219 9592

Outcome results

None listed

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