Actively Recruiting

Age: 18Years +
All Genders
NCT07315386

Catatonic Syndrome in Adult Patients at Basurto Hospital: A Descriptive Study of Incidence, Comorbidity, and Short-Term Outcomes

Led by Beatriz Rodriguez Cabo · Updated on 2026-05-12

40

Participants Needed

1

Research Sites

365 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to assess the incidence, sociodemographic and clinical characteristics, treatment response, and short-term outcomes of adult patients with catatonic syndrome in the Bilbao area (Spain). Data will be collected from January 2024 to December 2025 from all patients aged 18 years or older diagnosed with catatonia of any etiology at Basurto University Hospital who provide informed consent to participate.

CONDITIONS

Official Title

Catatonic Syndrome in Adult Patients at Basurto Hospital: A Descriptive Study of Incidence, Comorbidity, and Short-Term Outcomes

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age ≥ 18 years at the time of hospital care
  • Diagnosis of catatonic syndrome according to DSM-5 criteria
  • Patients attended at Basurto University Hospital in any clinical setting, including Emergency Department or inpatient physical or psychiatric units
  • Diagnosis made between 1 January 2024 and 31 December 2025
  • Catatonia of any cause, including psychiatric, neurological, medical, metabolic, toxic, or autoimmune
  • Provision of informed consent by patient or legal representative, with deferred consent allowed in acute cases
Not Eligible

You will not qualify if you...

  • Refusal to participate by patient or legal representative
  • Withdrawal of informed consent at any time during the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Beatriz Rodriguez Cabo

Bilbao, Vizcaya, Spain

Actively Recruiting

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Research Team

B

Beatriz Rodriguez-Cabo, Professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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