Parrot power: live and robotic birds ease needle pain in study
NCT ID NCT07241780
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether interacting with a live parrot, a robotic parrot, or a picture of a parrot could reduce pain during blood draws in 240 adults with chronic diseases. Participants were randomly assigned to one of the three groups, and their pain was measured using a standard scale. The goal was to see if a simple, non-drug distraction could help make a common medical procedure less painful.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Parrot therapy (live, robotic, or picture)
- What this could lead to
- If effective, parrot therapy could offer a simple, drug-free way to ease pain during medical procedures like blood draws.
- What could go wrong
- This is a small, completed study. The effect may be modest or not apply to other procedures or populations. Pain is subjective and results may vary.
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
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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
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240 people
The number who actually took part.
- Started
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Jul 2024
- Finished
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Aug 2024
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Individuals aged 18 years or older, * Literate, * Able to communicate verbally, * Without vision/hearing/speech problems, * With at least 6 months of chronic disease, * With a single venous access point, and who gave consent were included. Exclusion Criteria: * Refusal to give consent, * Psychiatric diagnosis, * Hemodynamic instability, * Presence of Chronic Obstructive Pulmonary Disease/Asthma, * Chronic disease duration of less than 6 months.
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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
-
Gümüşhane University
Gümüşhane, 29600, Turkey (Türkiye)
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