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Investigating the effect of Hop capsule on sleep quality of postmenopausal women

Investigating the effect of Hop capsule on sleep quality of postmenopausal women

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241221064121N1
Enrollment
112
Registered
2025-03-15
Start date
2025-04-05
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Sleep disorders. Sleep disorders

Interventions

Intervention 1: Intervention group: For people of this group, if they meet the inclusion criteria, after providing explanations about the thesis plan and obtaining informed consent before the interven

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Informed written consent to participate in the study Women aged 45-60 years At least one year has passed since the last menstrual period after the onset of natural menopause Obtaining a score greater than 5 in the Pittsburgh Sleep Quality Index (PSQI) and a score greater than 7 in the Insomnia Severity Index (ISI) Not having allergies to food, medicine or certain substances

Exclusion criteria

Exclusion criteria: Having known chronic diseases (heart, kidney, thyroid, blood pressure, diabetes, etc.) The use of hormone therapy of other herbal substances Consumption of alcohol and addictive drugs Using other traditional treatment methods and complementary medicine in the last 4 weeks Using medications that affect sleep (diuretics, sedatives, pain relievers, depression and anxiety medications) Induced menopause, i.e. bilateral oophorectomy or hysterectomy and artificial termination of ovarian function with chemotherapy and/or radiation therapy People with a score of more than 28 from the Beck questionnaire and more than 30 from the Hamilton questionnaire Suffering from sleep apnea

Design outcomes

Primary

MeasureTime frame
Sleep quality. Timepoint: Before the start of the intervention and 4 and 8 weeks after the start of the intervention. Method of measurement: Pittsburgh Sleep Quality Index Questionnaire and Insomnia Severity Index Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNahid Masoudi Ashtiani

Ahvaz University of Medical Sciences

masoudiashtiani.n@ajums.ac.ir+98 912 419 6775

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026