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Clinical Trials/IRCT2015062722939N1
IRCT2015062722939N1
Completed
未知

Comparison of the effect of face to face training and E-learning on the fatigue and maternal and baby’s quality of sleep in the postpartum period

Vice chancellor for research, Isfahan university of medical science0 sites120 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Fatigue and sleep disorder.
Sponsor
Vice chancellor for research, Isfahan university of medical science
Enrollment
120
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Vice chancellor for research, Isfahan university of medical science

Eligibility Criteria

Inclusion Criteria

  • inclusion criteria: People giving birth to live, singleton healthy, people who are breastfeeding (exclusive breastfeeding or with milk), No risk of bleeding during and after delivery (with the question of the mother), After delivery of the highest hospitalization was 3 days, having an underlying medical condition (asthma, kidney disease, congestive heart failure, gastroesophageal reflux disease, rheumatic disorders, joint pain and other musculoskeletal, diabetes) who are sleep disorders, Lack of depression during the study period (with the use of the Edinburgh Postnatal Depression Scale short\-be determined (according to the Edinburgh questionnaire, people who score less than 13 get\-out, depressed and those with scores equal to or greater than 13 acquire, they will be considered depressed), Married Women and Iranian nationality, no drug addiction and no Hypnotic drugs addiction (for example benzodiazepines), no repeated spontaneous abortions, no neonatal death, Non\-working mother; Exclusion criteria: Unwillingness to continue cooperation during the study, not completing the questionnaire completely and correctly, people who suffer from postpartum depression during the study (diagnosed with the information given to mothers at the beginning of the study), providing any disease or disorder that it effects on the sleep of the mother and infant during the study such as long\-term cold (more than three days), infectious diseases that cause fever, prolonged fever, hospitalization of the mother and infant, factors such as postpartum bleeding after the sampling.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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