Honest placebos: a new way to fight the opioid crisis?
NCT ID NCT06350786
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether giving people with chronic pain a placebo pill—told openly that it's a placebo—can help them safely reduce their opioid painkiller use. 86 participants will either receive the placebo alongside a mind-body program or just electronic monitoring for 6 weeks. The goal is to lower daily opioid doses and ease withdrawal symptoms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- open-label placebo pills
- What this could lead to
- If it works, this could offer a safe, non-drug way to help people cut down on opioid painkillers without increasing pain or withdrawal.
- What could go wrong
- This is a small early-stage trial with only 86 people. The placebo effect is unpredictable, and results may not apply to everyone. There is also a risk that pain or withdrawal symptoms could worsen.
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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About 86 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2024
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- 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.
Show the full entry requirements Hide 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: * Signed Informed Consent * ≥ 18 years of age * German speaking * Pain lasting ≥ 4 weeks, including subacute pain (4-12 weeks) and chronic pain (\>12 weeks) * Opioid medication for pain management for ≥ 4 weeks * Oral intake of opioid medication * Motivation for opioid reduction * Participants have a primary treating physician who performs the reduction of the opioid medication * Having access to a computer or tablet with an email-account Exclusion Criteria: * Having psychotic symptoms * Suicidality * Cognitive impairment to everyday life * Planned surgery within the next two months that is expected to affect opioid intake * Known illegal drug or harmful alcohol consumption * Intolerance of the ingredients of the placebo pill (e.g., lactose, sucrose, corn-starch) * Serious health problems that make study participation impossible * Simultaneous participation in other studies with investigational drugs or pain specific interventions
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Hospital Zurich, Department of Consultation-Liaison Psychiatry and Psychosomatic Medicine
RECRUITINGZurich, Canton of Zurich, 8006, Switzerland
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