Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
60 participants
INTERVENTIONAL
2021-01-01
2021-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Routine antenatal care
the control group will receive routine antenatal care and will not receive the guidelines group included 30 cases
No interventions assigned to this group
Ottawa guidelines
study group will receive routine antenatal care in addition to the Ottawa nutritional guidelines group included 30 cases
Acupressure and nutritional advices
Teaching using booklets and application of acupressure
Interventions
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Acupressure and nutritional advices
Teaching using booklets and application of acupressure
Eligibility Criteria
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Inclusion Criteria
2. gestational age of 7-13 weeks
3. singleton pregnancy
4. having a score of 7-12 on the (PUQE 24)
5. can read and write
6. having phone number
7. not receiving medications for reducing NVP, except for vitamin B6
8. wanted pregnancy.
Exclusion Criteria
2. occurrence of obstetric complications during the study
3. hyper-emesis gravidarum
4. having physical or mental disorders
5. having oral/speech impairments
6. having assisted reproductive techniques for the present pregnancy
7. having two consecutive miscarriages before the current pregnancy
8. old primigravida
9. narcotic use or alcohol drinking
10. and subjects who will show signs and symptoms of hyperemesis gravidarum during the study will be dropped out and referred to medical care.
22 Years
35 Years
FEMALE
No
Sponsors
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Cairo University
OTHER
Responsible Party
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Noura Mohamed Eltoukhy
Assistant lecturer
Principal Investigators
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Noura Mo Eltoukhi, PhD
Role: PRINCIPAL_INVESTIGATOR
Cairo University
Noura M Eltoukhi, lecturer
Role: PRINCIPAL_INVESTIGATOR
Faculty of Nursing Cairo University
Locations
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Faculty of Nursing
Cairo, , Egypt
Countries
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Provided Documents
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Document Type: Study Protocol, Statistical Analysis Plan, and Informed Consent Form
Other Identifiers
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IORG0003381
Identifier Type: -
Identifier Source: org_study_id
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