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Assessment of Lippia Citriodora effect on Sleep DisorderversusOilineffective: A double blind study

Assessment of Lippia Citriodora effect on Sleep DisorderversusOilineffective: A double blind study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016061528485N1
Enrollment
82
Registered
2016-12-23
Start date
2016-12-21
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

sleep disorder. Disorders of initiating and maintaining sleep [insomnias]

Interventions

Intervention 1: In the control group using vegetable oils in lemon and control groups using inert oil (liquid paraffin). Intervention 2: dropping two drops of inert oil in the nose morning and night.
Placebo
In the control group using vegetable oils in lemon and control groups using inert oil (liquid paraffin)
dropping two drops of inert oil in the nose morning and night

Sponsors

University of Welfare and Rehabilitation Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria (inclusion): Tendency to participate in the study? Having over 60 years old? Having sleep disorders, in self-reported, or clinical level, and according to the Pittsburgh questionnaire? Ability of respond to the questionnaire? No history of any allergy, to lemon verbena, or mangroves plants? No continuous using from (twice or more in per week) from lemon Herbal Tea, or lemon extract over 1 month ago? No problems with the airway and nasal obstruction Exclusion criteria (exclusion): Having dependence or addiction to alcohol , drugs and medicines? Having disease, like that heart failure, respiratory disorders, and diseases of sleep, and wake-up cycle such as, respiratory apnea, and restless leg syndrome? Using from Effective drugs, on the sleep and wake up cycle (except previous prescribed drugs )

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Improve sleep quality. Timepoint: Intervention. Two weeks after starting treatment and after the treatment (4 weeks after the intervention). Method of measurement: questionnaire.

Secondary

MeasureTime frame
Improve sleep Subjective quality. Timepoint: Early intervention. 2 weeks after starting intervention and 4week after intervention. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyran mohamadi bolban abad

University of Welfare and Rehabilitation Research Center

mohammadi162@yahoo.com se.mohamadi@uswr.ac.ir+98 21 2218 0154

Outcome results

None listed

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