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Determining the effect of educational application on sleep disorders in postmenopausal women

Design, implementation and evaluation of an educational application to improve sleep disorders in postmenopausal women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240906062963N1
Enrollment
60
Registered
2024-10-01
Start date
2024-11-11
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Sleep Disorder. Sleep disorders

Interventions

Intervention group: We run the educational application for improving sleep disorder on the mobile phone of one of the participants in the intervention group to ensure that it works properly. After ins

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in the project and have a written consent Obtaining a score lower than the cut-off point in the sleep disorder questionnaire The duration of menopause is 1-5 years Reading and writing literacy Having a smart phone Getting to know how to use a smart phone

Exclusion criteria

Exclusion criteria: People with a score of more than 29 from the Beck questionnaire and more than 30 from the Hamilton questionnaire Having a chronic disease leading to insomnia, such as rheumatoid arthritis The presence of known mental illnesses History of frequent use of sleeping pills History of frequent use of sleeping pills Major stressors in the last 3 months such as loss of loved ones and divorce Employment in jobs with shift work, especially night work People with a BMI >30 People with a score of more than 29 from the Beck questionnaire and more than 30 from the Hamilton questionnaire

Design outcomes

Primary

MeasureTime frame
Improving indicators of sleep disorders. Timepoint: Before starting the intervention and The beginning of the intervention 4 and 8 weeks after using the application. Method of measurement: Insomnia Severity Index Questionnaire, Pittsburgh Sleep Quality Index Questionnaire, daily sleep data registration form.

Secondary

MeasureTime frame
Anxiety score. Timepoint: Before the intervention and 4 and 8 weeks after using the application. Method of measurement: Hamilton anxiety questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPoorandokht afshari

Ahvaz University of Medical Sciences

p_afshary@yahoo.com+98 61 3373 8619

Outcome results

None listed

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