Inside the hoarding brain: can scans reveal why letting go is so hard?
NCT ID NCT03487224
First seen Aug 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time
Summary
This study uses brain scans to explore how people with hoarding disorder make decisions compared to healthy individuals. Participants will perform cognitive tasks while undergoing fMRI, which measures brain activity by tracking blood flow. The goal is to identify differences in brain regions involved in decision-making that may contribute to hoarding behaviors.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Functional magnetic resonance imaging (fMRI) with cognitive tasks
- What this could lead to
- If successful, this could reveal how brain activity during decision-making differs in hoarding disorder, potentially guiding future treatments.
- What could go wrong
- This is a small, early-stage brain imaging study, not a treatment trial. It may not capture the full complexity of hoarding disorder or lead directly to clinical changes.
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.
- Participants
-
About 25 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jul 2018
- Expected to finish
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May 2027
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.
Who is studied
Individuals with Hoarding Disorder and Healthy Participants
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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.
Identify inclusion criteria. Inclusion criteria for participants diagnosed with HD: 1. ages 18-70 2. primary diagnosis of hoarding disorder 3. sufficient severity of hoarding symptoms 4. stable on psychotropic medications for 1 month prior to study enrollment 5. capacity to provide informed consent 6. ability to tolerate clinical study procedures Inclusion criteria for healthy control participants: 1. ages 18-70 2. capacity to provide informed consent Identify exclusion criteria. Exclusion criteria for participants with HD: 1. psychiatric or medical conditions that make participation unsafe 2. pregnant or nursing females 3. concurrent use of any medications that might increase the risk of participation (e.g. drug interactions) 4. presence of metallic device or dental braces Exclusion criteria for healthy control participants: 1. any current or lifetime psychiatric diagnosis 2. current or past use of psychotropic medication 3. pregnant or nursing females 4. major medical or neurological problem 5. presence of metallic device or dental braces
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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
-
Stanford University
Stanford, California, 94305, United States
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Other studies related to the condition(s) this trial covers.
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