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Simple thumb pressure before injections may ease pain and fear

NCT ID NCT07505992

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether applying acupressure to a specific point on the hip for one minute before an intramuscular injection could reduce pain, fear, and improve satisfaction. Sixty-eight adults receiving a diclofenac shot were randomly assigned to acupressure or standard care. The goal was to see if this simple, drug-free technique makes injections more comfortable.

What this could mean

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

Active substance
acupressure
What this could lead to
If it works, this could provide a simple, non-drug way to reduce pain and fear during injections, improving patient experience.
What could go wrong
This is a small, completed trial with only 68 participants. Results may not apply to all patients or settings, and the effect may be modest.

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

68 people

The number who actually took part.

Started

Nov 2024

Finished

Feb 2025

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 years and older

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: * Were aged 18 years or older, * Possessed sufficient physical and cognitive abilities to assess pain using the VAS, * Had the ability to read and comprehend study instructions, * Were newly prescribed IM Diclofenac Sodium (without prior doses), * Had a body mass index within the normal or obese range ac- cording to WHO classification, * Had no scars, wounds, Exclusion Criteria: Patients who had taken any analgesic medications on the day of injection were excluded.

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Conditions

The condition(s) this trial relates to.

anxiety disorder Pain Personal Satisfaction

As listed by the trial registrant

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

Contacts and locations

Locations

  • Eastern Mediterranean University

    Famagusta, 34381, Cyprus

More trials for these conditions

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