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Articles

Comparison of the effect of lavender and bitter orange on sleep quality in postmenopausal women: A triple-blind, randomized, controlled clinical trial

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Pages 851-865 | Received 25 Oct 2016, Accepted 26 Jun 2017, Published online: 25 Aug 2017
 

ABSTRACT

This trial compared the effects of lavender and bitter orange on sleep quality in postmenopausal women. This trial was conducted in 2015. Eligible postmenopausal women were allocated into one of two intervention groups or a control group (n = 52 per group) in a 1:1:1 ratio using a randomized block design. Intervention groups received 500 mg capsules containing only bitter orange or lavender flower powder, and the control group received 500 mg capsules containing starch. The Pittsburgh Sleep Quality Inventory was used before and eight weeks after starting the intervention. Data analyses were based on intention to treat. A one-way ANOVA showed a slightly significant difference in mean sleep score among the three groups before the intervention (p = .045). The general linear model, adjusted for baseline sleep score and confounding factors, showed significant differences among the groups in the mean sleep score after eight weeks of treatment (p < .001). Bitter orange and lavender significantly improved the mean sleep score compared with the control group (p < .001 and p = .003, respectively). The positive effect of bitter orange and lavender on sleep quality in postmenopausal women suggests that they can be used to improve sleep quality in such women.

Acknowledgments

This article is based on a master’s thesis in midwifery Department of Nursing and Midwifery faculty of Tabriz University of Medical Sciences approved by the Regional Ethics Committee of Tabriz University of Medical Sciences under the ethical code 1394.98. Authors would like to thank the assistance and financial support of the Research Deputy of Tabriz University of Medical Sciences. Authors also appreciate the assistance of authorities and personnel of the clinics of Imam Reza and Fatemiyeh Hospitals in West Azerbaijan Province, Iran and the cooperation of participants.

Clinical trial registration

This study was approved by Ethics Committee of Tabriz University of Medical Sciences (code: 9498) and registered at the Iranian Registration Clinical Trial centre (code: IRCT201504236582N11).

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