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Touch therapy tames Pre-Surgery jitters in bladder surgery patients

NCT ID NCT05325307

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study tested whether acupressure, a technique that applies gentle pressure to specific points on the body, can lower anxiety and steady vital signs in people about to have bladder removal surgery (cystectomy). Sixty adults participated, and researchers measured their anxiety levels and things like heart rate and blood pressure before and after the treatment. The goal was to see if this simple, non-drug method could help patients feel calmer before a major operation.

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

Oct 2022

Finished

Dec 2024

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

18 to 65 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Agreeing to participate in the research (signing the Informed Consent Form), * Conscious and cooperative * Speaks and understands Turkish, * 18-65 years old, * Before surgery, * Stable general condition, * No sensitivity in the area where acupressure/placebo acupressure will be applied, * 15 July 2022 - 15 July 2023 hospitalized in the urology clinic, * No active COVID-19 infection, * Patients without any psychiatric diagnosis will be included. Exclusion Criteria: * Those who do not agree to participate in the research (who do not sign the Informed Consent Form) * Conscious and uncooperative, * Not speaking or understanding Turkish, * Not between the ages of 18-65, * No surgical intervention planned, * The planned emergency surgical intervention, * Unstable general condition, * Sensitivity in the area where acupressure/placebo acupressure will be applied, * Active COVID-19 infection, * 15 July 2022 - 15 July 2023 who did not stay in the urology clinic, * Patients with current psychiatric diagnosis will not be included in the study.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Turkey, Mersin University,

    Mersin, Turkey/Mersin,Yenişehir, 33343, Turkey (Türkiye)

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Other studies related to the condition(s) this trial covers.