Abstract | OBJECTIVE: DESIGN: Double-blind, placebo-controlled study. SUBJECTS: 97 women with mean gestational length completed 8-12 weeks. MAIN OUTCOME MEASURES: Symptoms were recorded according to intensity, duration and nature of complaints. RESULTS: 71% of women in the intervention group reported both less intensive morning sickness and reduced duration of symptoms. The same tendency was seen in the placebo group, with 59% reporting less intensity and 63% shorter duration of symptoms. However, a significance level of 5% was reached only in the case of duration of symptoms, which was reduced by 2.74 hours in the intervention group compared to 0.85 hours in the placebo group (p = 0.018). CONCLUSIONS:
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Authors | A J Norheim, E J Pedersen, V Fønnebø, L Berge |
Journal | Scandinavian journal of primary health care
(Scand J Prim Health Care)
Vol. 19
Issue 1
Pg. 43-7
(Mar 2001)
ISSN: 0281-3432 [Print] United States |
PMID | 11303547
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Acupressure
(instrumentation, methods)
- Adult
- Ambulatory Care
(methods)
- Double-Blind Method
- Female
- Humans
- Nausea
(therapy)
- Norway
- Placebos
- Pregnancy
- Pregnancy Complications
(therapy)
- Self-Assessment
- Urban Population
- Wrist
(physiology)
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