comparison of aromatherapy with Citrus aurantium and lavender on sexual satisfaction of lactating wome
- Conditions
- sexual satisfaction.
- Registration Number
- IRCT20160427027633N3
- Lead Sponsor
- Kermanshah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 210
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
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sexual satisfaction. Timepoint: Before and 40 days after the intervention. Method of measurement: Lindaberg's Sexual Satisfaction Questionnaire.
- Secondary Outcome Measures
Name Time Method Side effects. Timepoint: 40 days after start the intervention. Method of measurement: Researcher made questionnaire.