Efficacy and Safety of Auricular Acupressure for Perimenopausal Insomnia
Starting soon · Not applicable · Has a placebo group
Conditions studied: Perimenopausal Insomnia
In brief
Perimenopausal insomnia is a condition where women frequently experience poor sleep around the time of perimenopause due to perimenopausal syndrome. It mostly affects women aged 40 to 55. Compared to primary insomnia, this type has the highest incidence and comes with complex physiological and hormonal changes. Insomnia during this phase is more than just a sleep problem; it is often accompanied by symptoms like hot flashes and night sweats, which have a broad negative impact on women's physical and mental well-being. Therefore, finding effective treatment strategies is especially important. Currently, the main treatments for perimenopausal insomnia include cognitive therapy, hormone replacement therapy (HRT), and sedative-hypnotic drugs. As first-line options, cognitive therapy and HRT are widely recognized for their positive effects on improving sleep. However, long-term use of these medications can lead to dependency and increase the risk of endometrial cancer, breast cancer, stroke, and coronary heart disease. As a result, finding a safe and effective non-drug alternative is highly meaningful. At present, there is still a lack of high-quality research evidence to fully confirm the exact efficacy of auricular acupressure for perimenopausal insomnia.
Key facts
- Study ID
- NCT07708324
- Run by
- The First Affiliated Hospital of Zhejiang Chinese Medical University
- People needed
- 98
- Starts
- 2026-07-01
- Expected to finish
- 2027-08-31
- Last updated by the study team
- 2026-07-16
Who can join
Age: 40 and older, up to 55. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Female, aged 40-55 years.
- Meets the STRAW criteria for perimenopause.
- Meets DSM-5 diagnostic criteria for insomnia disorder.
- Insomnia symptoms have persisted for at least 4 weeks.
- Has not used insomnia medication or has received a stable dose for at least 2 months.
- Has not previously received auricular acupressure.
- Able to comply with study procedures.
- Provides written informed consent.
You may not qualify if…
- Pregnancy or lactation.
- Premature ovarian insufficiency.
- Surgical menopause.
- Insomnia secondary to neurological disease.
- Major psychiatric disorders.
- Alcohol or substance abuse.
- Skin infection at auricular sites.
- Participation in another clinical trial within the previous 3 months.
- Chronic pain disorders affecting sleep.
Full record on ClinicalTrials.gov
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