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Can a cold pack on your wrist and ankle cool menopause symptoms?

NCT ID NCT07533097

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Aug 14, 2026 · Updated 2 times

Summary

This study will test whether applying cold gel packs to two specific acupoints (LI4 on the hand and SP6 on the leg) can reduce hot flashes and depression in women going through menopause. About 80 women with daily hot flashes will be randomly assigned to receive the cold pack treatment or not. Researchers will measure changes in hot flash impact and depression symptoms using standard questionnaires.

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

60 people

The number who actually took part.

Started

Apr 2026

Finished

Aug 2026

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

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: * In the perimenopausal phase (no menstruation for 3-11 months or an increase in irregular menstrual bleeding) or the postmenopausal phase (no menstruation for more than 12 months), * Participants experiencing moderate to severe hot flushes at least four times a day in the week prior to enrolment, * Participants who are literate in Turkish and able to communicate, * Participants who volunteer to take part in the study will be included in the study. Exclusion Criteria: * Women who have entered menopause following surgery, * Women whose hot flush symptoms have decreased or ceased in the week prior to joining the study, * Those receiving hormone replacement therapy, * Those who had received herbal medication (such as black cohosh, black cohosh, ginkgo, ginseng, motherwort, valerian, black snake root, St. John's wort, etc.) or chemical medication for at least two weeks prior to joining the study, * Women with endocrine system disorders such as diabetes or a condition presenting symptoms similar to hot flushes, * Women with a regular menstrual cycle, * Women with a psychiatric diagnosis who are currently receiving treatment, * Women taking sleeping pills, * Women with a language barrier preventing communication in Turkish, * Women who are not willing to participate in the study will not be included in the research.

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Conditions

The condition(s) this trial relates to.

Hot Flashes

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Başkent Üniversitesi Hastanesi

    Ankara, Turkey (Türkiye)

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