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The impact of Myo-inositol supplementation with sleep hygiene education on sleep quality in pregnant women

The impact of Myo-inositol supplementation with sleep hygiene education on sleep quality in pregnant women

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160208026446N3
Enrollment
60
Registered
2018-06-03
Start date
2018-04-07
Completion date
Unknown
Last updated
2019-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep quality in pregnancy. Sleep disorders

Interventions

Intervention 1: Intervention group: myoinositol supplementation powder the ino folic commercial name containing 2000 mg of myoinositol and 200 µg of folic acid (manufactured by the company Lo.Li Pharm

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Conscious written consent Pregnant women with singletone pregnancy Age 18 and over Gestational age of 14 weeks Absence of chronic physical diseases such as diabetes, high blood pressure and cardiovascular disease No history of taking prenatal drugs before pregnancy No history of sleep disorders before pregnancy Working women without night shift work Non-smoking and alcohol Lack of history of psychiatric use No history of abortion in previous pregnancies

Exclusion criteria

Exclusion criteria: Severe depression or severe stress Death experience of one of the first-degree relatives during pregnancy Changes in sleep status due to travel

Design outcomes

Primary

MeasureTime frame
Sleep Quality Score in Pittsburgh Sleep Quality Questionnaire. Timepoint: In the second trimester of pregnancy at weeks 24 to 28 and in the third trimester of pregnancy at weeks 37 to 38 of pregnancy. Method of measurement: Pittsburgh Sleep Quality Index Questionnaire.

Secondary

MeasureTime frame
Neonatal and pregnancy outcomes. Timepoint: The end of pregnancy for the outcome of pregnancy and infancy Method of measurement. Method of measurement: Questionnaire and complete the checklist using file.;Side effect of drug. Timepoint: In the second trimester of pregnancy (week 24-28) and the third trimester of pregnancy (week 37_38). Method of measurement: Drug side effect checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMolood Aghajani Delavar

Babol University of Medical Sciences

moloodaghajani@yahoo.com+98 11 3236 0714

Outcome results

None listed

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