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Ear acupressure may offer Drug-Free sleep relief for menopausal women

NCT ID NCT07708324

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time

Summary

This trial investigates whether auricular acupressure—applying small seeds to pressure points on the ear—can safely improve sleep in women aged 40 to 55 who have insomnia during perimenopause. Participants will receive either real acupressure or a sham version, and sleep quality will be measured using questionnaires and sleep diaries. The goal is to find a non-drug alternative that avoids the risks of hormone therapy or sleeping pills.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
auricular acupressure using adhesive plasters containing Vaccaria seeds
What this could lead to
If effective, this could offer a safe, non-drug option for improving sleep in women with perimenopausal insomnia, avoiding risks linked to hormone therapy or sedatives.
What could go wrong
This is a small, early-stage trial with 98 participants, and the sham control may reveal only a modest benefit. Results may not apply to all women or confirm long-term safety.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 98 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Aug 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

40 to 55 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * 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. Exclusion Criteria: * 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.

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