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Study aim: Determining and comparing the effect of lavender and clove essential oil on the intensity of pain and anxiety in the first stage of labor Design: Clinical trial with control group, with parallel groups, single blind, phase3 on 159 people, random block allocation of samples Settings and conduct: The study will be conducted in the maternity hospitals of AllamehBahloul Gonabadi Gonabad and Hashminejad Hospitals in Mashhad.After explaining and obtaining informed consent, the eligible samples are randomly divided into three aromatherapy groups with lavender, cloves and distilled water (control group).Completion of individual and midwifery questionnaires and checklist of observation and examination and aromatherapy are performed in 4-5 cm dilatation by connecting gauze impregnated with 0.2 cc of 2% solution to the collar of the samples and repeating every 15 minutes.Pain intensity(VAS) and anxiety intensity(Spielberger) are measured twice at 4-5cm dilation and 8-10cm dilation.The samples are blind of the prescribed essential oil type. Participants/Inclusion and exclusion criteria: Inclusion criteria: -Women with first and second pregnancy -Having informed consent -Gestational age 38-42w -Cervix dilatation more than 3cm -Normal Vaginal Delivery -No history of asthma, allergy and sensitivity to herbal medicines and smell problems -Absence of pregnancy and obstetrics complications -Not suffering from known anxiety and depression and migraine -Not receiving medical painkillers 3 hours before the start of the intervention Exclusion criteria: -Non-cooperation of the mother -Leaving the natural course or emergency caesarean section -Allergic to essential oil Intervention groups: Three intervention groups include aromatherapy with lavender essential oil, clove essential oil and distilled water Main outcome variables: Intensity of pain and anxiety in the first stage of childbirth
IRCTID: IRCT20230301057585N1
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