Sleep disorders. Other nonorganic sleep disorders
Conditions
Interventions
Intervention 1: The control group will receive one Placebo tablet every fortnight for 2 months. These tablets contain edible paraffin oil. Intervention 2: The intervention group Will receive 50000 uni
Placebo
Treatment - Drugs
The control group will receive one Placebo tablet every fortnight for 2 months. These tablets contain edible paraffin oil.
The intervention group Will receive 50000 units of vitamin D tablets, one tablet every fortnight for 2 months.
Sponsors
Vice chancellor for research, Ahvaz Jundishapur University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Personal willingness to participation; Aging 20 to 50 year old; Suffering sleep disorder based on Pittsburgh Sleep Quality Index; No allergy to vitamin D supplement; No mental psychic disorder; No consumption of sleep medication or anti-depression; No consumption of vitamin D supplement three months before intervention. Exclusion criteria: Allergy to vitamin D supplement; Consumption of sedative drugs; Suffering mental problems such as hyper-depression or excessive anxiety; Pregnancy or lactation; Drinking or smoking; Lack of willingness to participation.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sleep quality. Timepoint: Before intervention and 2 months afther intervention. Method of measurement: Pittsburgh Sleep Quality Index. | — |
Secondary
| Measure | Time frame |
|---|---|
| 25 Hydroxy Vitamin D3 Serum. Timepoint: Before intervention and 2 months after intervention. Method of measurement: ELISA. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHosseini Seyed Ahmad
Ahvaz Jundishapur University of Medical Sciences
Outcome results
None listed