Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
500
Sex
Women only
Ages
Ages 45 Years to 60 Years
Primary completion
2026-03-01
Last update
2025-12-23

What this trial studies

This study aims to evaluate the effects of sleep hygiene education on sleep quality and depression in women during menopause. Women will be randomly assigned to either an education group or a control group. The education group will receive training based on the Information-Motivation-Behavioral Skills (IMB) Model. Sleep quality and depression levels will be measured before and after the education.

Conditions in scope

  • Insomnia
  • Depressive Symptoms

Interventions

  • Sleep Hygiene Education (Behavioral) — Education based on the IMB Model targeting sleep habits, routines, and sleep hygiene behaviors to improve sleep quality.

Who can join

Women only · Ages 45 Years to 60 Years

Inclusion criteria

  • Being in menopause
  • Being between 40 and 60 years of age
  • Having a low sleep quality score according to the Menopause-Specific Sleep Quality Scale.
  • Being willing to participate in the study.
  • Having no physical or mental disabilities that would hinder communication.
  • Having technology (smartphone, tablet, or computer) with internet access and the ability to participate in online training.

Exclusion criteria

  • Having a history of receiving psychological support.
  • Having been diagnosed with a chronic psychiatric illness (previously diagnosed depression, anxiety disorder, etc.).
  • Having a neurological or chronic systemic illness that may affect sleep quality.
  • Being treated for a sleep disorder (receiving medication or psychotherapy).
  • Receiving hormone replacement therapy (HT).
  • Having received sleep hygiene training/therapy within the last 6 months.

Eligibility wording paraphrased from the public record. View the full criteria on ClinicalTrials.gov before contacting a site.

Where it’s happening

CityState / RegionFacilitySite status
Ankara Ankara Atatürk Sanatorium Training and Research Hospital Recruiting

Status & timeline

  • Overall status: Recruiting
  • Study type: Interventional
  • Phase: N/A
  • Start date: 2026-01-01
  • Primary completion: 2026-03-01
  • Last update posted: 2025-12-23
  • First posted: 2025-12-23

Lead sponsor: Ankara Yildirim Beyazıt University (Other)

For trial site contact information, use the official record at ClinicalTrials.gov. Contact details change frequently and the public record is the source of truth.

Outcome measures

Primary outcomes

  • Sleep Quality (Baseline and 10 weeks after intervention)
    Change in sleep quality measured using the Menopause-Specific Sleep Quality Scale before and after the sleep hygiene education intervention.

If you’re reading this trial because you have menopause symptoms now, you don’t have to wait for a trial to access evidence-based care. ClearedRx prescribes the same FDA-approved and compounded HRT products that have been studied in trials like this one for decades.

Important. Information from ClinicalTrials.gov as of May 8, 2026. Trial details (status, sites, contacts, eligibility, outcomes) change frequently — always check the official record at https://clinicaltrials.gov/study/NCT07299903 before contacting a site.

ClearedRx is not affiliated with this trial or its sponsor. We index public-domain ClinicalTrials.gov records to help patients find evidence-based context for menopause care decisions. ClearedRx itself is a telehealth menopause/HRT brand — we do not enroll patients in trials.