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Effect of Salvia Officinalis aroma on severity of Labor pain and anxiety

Effect of Salvia Officinalis aroma on severity of Labor pain and anxiety

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016042727633N1
Enrollment
160
Registered
2016-05-15
Start date
2015-09-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Abdominal and pelvic pain. Condition 2: Anxiety. pain localized to other parts of lower abdomen anxiety disorder unspecified/anxiety NOS

Interventions

Intervention 1: In the intervention group three drops of Salvia Officinalis fragrance were poured on a cotton and is connected to the cloths collar of samples and it repeated ever
Treatment - Drugs
Placebo
In the intervention group three drops of Salvia Officinalis fragrance were poured on a cotton and is connected to the cloths collar of samples and it repeated every half hour
In the contorol group three drops of normalsalin were poured on a cotton and is connected to the cloths collar of samples and it repeated every half hour

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: nclusion criteria: gestational age 42-38 weeks; with a singleton live fetus and cephalic presentation and approved by ultrasound; Examination of cervical dilatation on arrival 4-3 cm; without any medical problems or complications of pregnancy and mental illness; lack of respiratory diseases and allergies; having tested positive smell; lack of drug addiction and alert in time and place. The exclusion criteria were: mother's unwillingness to continue to participate in the study; occurrence of Any difficulties during the study(such as cord prolapse; placental abruption; preeclampsia , etc.); receive analgesic 3 hours before the intervention and decreaseof consciousness.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Before the intervention, and at 7-5 cm dilatation. Method of measurement: Scale (STAI).;Pain. Timepoint: Before the intervention and dilatations of 3-4, 5-7 and 8-10 cm. Method of measurement: VAS.

Secondary

MeasureTime frame
Apgar of newborn. Timepoint: The first and fifth minutes after birth. Method of measurement: Scale five of determination of Apgar.;Time of first Stage of Labor. Timepoint: In dilatation of 4-3, 7-5 and 10-8 cm. Method of measurement: duration and interval of conteractions, dilatation and effacement of cervix.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFrozan sharifipour

Kermanshah University of Medical Sciences, School of Nursing and Midwifery

sharifipour_fr91@yahoo.com+98 83 3828 2101

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026