sexual satisfaction.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: willingness to participate in the study having health dossier in health care centers literacy sufficient to complete of the questionnaire married and lives with her husband permanently use a reliable method of contraception exposure during lactation (6-3 months postpartum) lack of mental health problems or known systemic disease affecting a person's sexual function lack of drug dependence lack of sexual problems in husband according wife's comment lack of addicted husband the absence of stressful events in the last 6 months (divorce of parents, death of family members, etc.) the absence of diseases, , lack of stress factors (Parent divorce in the past six months), l the lack of any effective drug on a person's sexual response (Antihypertensive drugs, Thiazide Diuretics, Antidepressants, Antihistamines, Barbiturates, Narcotics, Diazepins, Amphetamines, Cocaine) lack of disorder of olfactory or sensitivity to herbal medicines according wife's comment and other disorders related to nose (fracture, deviated septum, rhinitis and sinusitis
Exclusion criteria
Exclusion criteria: dissuasion of participating in the study incidence of side effects and sensitivity to essential oils during the study emotional major event such as a death of One of the relatives in particular loss of child proof of pregnancy occurrence during the study the incidence of mental health problems or serious illness during the study living away from his husband catching the debilitating diseases such as cancer that person will have to leave the study surgery during the intervention divorce,death or illness of husband during the intervening period of study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual satisfaction. Timepoint: Before and 40 days after the intervention. Method of measurement: Lindaberg's Sexual Satisfaction Questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Side effects. Timepoint: 40 days after start the intervention. Method of measurement: Researcher made questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
School of Nursing and Midwifery