Loneliness may speed aging in schizophrenia, study suggests
NCT ID NCT07419321
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether social isolation contributes to the early health problems seen in people with schizophrenia, who often die 10–20 years earlier than others. Researchers will follow 650 participants (500 with schizophrenia and 150 siblings) aged 40–70, tracking medical records and social activity over time. The goal is to understand how loneliness impacts physical health and to guide future treatments that could reduce early death.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 650 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2024
- Expected to finish
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Jul 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
500 clinically stable schizophrenia participants, and 150 of their unaffected siblings from a list of eligible participants of large existing studies of schizophrenia: e.g. EUropean network of national schizophrenia networks studying Gene-Environment Interactions (EU-GEI) and large scale research studies that took place at the Olin Neuropsychiatry Research Center, Institute of Living, Hartford, CT. All participants consented to be recruited for future studies.
- Ages
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40 to 70 years
- Sex
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Anyone
- Healthy volunteers
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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.
Inclusion and exclusion criteria for participants with SZ: * DSM-IV or V diagnosis of a SZ related disorder (295.x, 297.1, 298.8, or 298.9; e.g., schizophrenia, schizoaffective disorder, schizophreniform disorder, but not psychotic disorder that is solely substance induced) based on clinical interview; * Between 40 and 70 years of age at time of study recruitment; * Participant was enrolled in a previous research study between the ages of 20-55, and this study took place at least 5 years ago; * Able to understand the spoken language of the participating country sufficiently to comprehend testing procedures; * No history of serious head injury (i.e., loss of consciousness longer than 1 hour, no neuropsychological sequelae, no cognitive rehabilitation treatment post head injury); * No history of IQ \< 70, or developmental disability based on chart review; * Clinically stable (i.e., no inpatient hospitalizations for three months prior to enrollment, no changes in medication in the four weeks prior to enrollment; The inclusion and exclusion criteria for sibling participants in this study will be: * No history of any DSM IV/V Axis I or axis II diagnosis that is known to be associated with social functioning (e.g. severe mood disorder, schizoaffective personality disorder, autism spectrum disorder); * Between 40 and 70 years of age at time of study recruitment;; * Participant was enrolled in a previous research study between the ages of 20-55, and this study took place at least 5 years ago; * Able to understand the spoken language of the participating country sufficiently to comprehend testing procedures; * No history of serious head injury (i.e., loss of consciousness longer than 1 hour, no neuropsychological sequelae, no cognitive rehabilitation treatment post head injury); * No history of IQ \< 70, or developmental disability based on chart review; * Clinically stable (i.e., no inpatient hospitalizations for three months prior to enrollment, no changes in medication in the four weeks prior to enrollment
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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
4 sites in 4 countries. 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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AUMC, University Hospital
RECRUITINGAmsterdam, North Holland, 1105AZ, Netherlands
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Hospital General Universitario Gregorio Marañon
RECRUITINGMadrid, 28030, Spain
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King's College London
RECRUITINGLondon, Se58AF, United Kingdom
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Olin Neuropsychiatry Research Center, Hartfort
RECRUITINGHartford, Connecticut, 06106, United States
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Other studies related to the condition(s) this trial covers.
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