Anxiety Level. Anxiety disorder, unspecified
Conditions
Interventions
Intervention 1: In test one (oil of orange peels) and experimental group II (Essence Geranium), on fabric, non-absorbent, the clothing connected. Before and 20 minutes after intervention anxiety inven
Prevention
Placebo
In test one (oil of orange peels) and experimental group II (Essence Geranium), on fabric, non-absorbent, the clothing connected. Before and 20 minutes after intervention anxiety inventory STAI, physi
In the control group, distilled water onto non-absorbent fabric, the clothing connected. Before and 20 minutes after intervention STAI anxiety questionnaire, physiological parameters were recorded by
Sponsors
Medical Sciences of Vice chancellor for research, North Khorasan University
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: included nulliparous women; full-term pregnancy (37-42); ages 18-35; with a single fetus; dilatation of3-5 cm ; haven't chronic disease; no colds and haven't nasal congestion; anosmia; lack of sensitivity to smell specific experience of breath smells particular (which bad recalls memories or stress); the use of sedatives or anti-anxiety in 3 hours before the experiment; no known mental illness; no history of epilepsy and asthma; lack of fetal distress; failure to induce labor there was a high risk pregnancy. Exclusion criteria for the study; the firm's unwillingness to continue the study of fetal distress or impairment in labor progress during the intervention; use of pain medication during labor induction or intervention
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anxiety level of first phase of labor. Timepoint: Befor and 20 min after intervention. Method of measurement: Spielberger state-trait. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pulse rate. Timepoint: Before and 20 minutes after intervention. Method of measurement: examination.;Systolic BP. Timepoint: Before and 20 minutes after intervention. Method of measurement: examination.;Diastolic BP. Timepoint: Before and 20 minutes after intervention. Method of measurement: examination.;Pain intensity. Timepoint: Before and 20 minutes after intervention. Method of measurement: VAS pain scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaboobeh Tabatabaee Chehr
North Khorasan University of Medical Sciences
Outcome results
None listed