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The effect of P6 Acupressure on nausea and vomiting of pregnancy

Not Applicable
Conditions
ausea and Vomiting of Pregnancy.
Registration Number
IRCT20190205042624N1
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
63
Inclusion Criteria

Mild to moderate nausea and/or vomiting
planned and normal pregnancy
gestational age under 20 weeks
Being literate

Exclusion Criteria

symptoms of Hyperemesis Gravidarum (weight loss, hydration therapy, intravenous drugs, and or hospitalization for treatment of NVP)
molar or twin pregnancy
threatened abortion
being affected by any known medical condition that might manifest with nausea or vomiting
history of recent psychological disorders which require referring to psychologist or psychiatrist or disastrous events
taking medicine (emetic or antiemetic)
smoking

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ausea of Pregnancy. Timepoint: Twice a day (midday and at night before bed) during the three days of intervention period. Method of measurement: Daily diaries form included frequency, duration (minute), and severity of nausea [scored from 0 (no nausea) to 4 (very severe nausea)] and frequency of vomiting.;Vomiting of Pregnancy. Timepoint: Twice a day (midday and at night before bed) during the three days of intervention period. Method of measurement: Daily diaries form included frequency of vomiting.
Secondary Outcome Measures
NameTimeMethod
Overall rate of response to treatment for nausea and vomiting. Timepoint: after intervention. Method of measurement: Questionnaire (overall rate of response to treatment for nausea and vomiting separately [scored from 0 (significantly worse) to 4 (significantly better)]).;Applying dietary modification. Timepoint: after intervention. Method of measurement: Questionnaire (applying dietary modifications (yes, almost, no)).;Satisfaction from treatment. Timepoint: after intervention. Method of measurement: Questionnaire (satisfaction from treatment (yes, almost, no)).
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