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Investigating the effect of circadian rhythm personalization program on improving the sleep quality of pregnant women and postpartum depression: a randomized field trial study

Investigating the effect of personalizing the circadian rhythm program in improving the sleep quality of pregnant women and postpartum depression

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200405046961N1
Enrollment
84
Registered
2024-08-22
Start date
2024-08-21
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Mental and behavioural disorders associated with the puerperium. Puerperal psychosis

Interventions

Intervention 1: During the first week, the members of the experimental group will learn about the topic and content of the study
In this way, they will participate in one-hour training sessions and learn scientific information in simple language about the circadian clock and its effect on health and psychiatric disorders, inclu

Sponsors

Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
21 Years to 40 Years

Inclusion criteria

Inclusion criteria: Age 21 to 40 years First pregnancy singleton pregnancy Pregnant women in the third trimester of pregnancy (between 25 and 27 weeks of pregnancy) receiving spouse's support at an average level (according to Sherbourne & Stewart's social support questionnaire) Sign the informed consent form in order to participate in the research

Exclusion criteria

Exclusion criteria: Age 21 to 40 years First pregnancy singleton pregnancy Pregnant women in the third trimester of pregnancy (between 25 and 27 weeks of pregnancy) receiving spouse's support at an average level (according to Sherbourne & Stewart's social support questionnaire) Sign the informed consent form in order to participate in the research

Design outcomes

Primary

MeasureTime frame
Sleep disorders of pregnant women. Timepoint: Before and after the intervention. Method of measurement: Pregnant Women's Sleep Disorders Questionnaire and Munich Chronotype Questionnaire.

Secondary

MeasureTime frame
Postpartum Depression. Timepoint: two and six weeks after delivery. Method of measurement: Edinburgh Postpartum Depression Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTayebeh Mohtashami

Shahroud University of Medical Sciences

t.mohtasham@gmail.com+98 23 3239 5054

Outcome results

None listed

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