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Competence Ability Study in People With Schizophrenia (CompSchizo)

T

Taichung Veterans General Hospital

Status

Unknown

Conditions

Competence
Schizophrenia

Treatments

Other: Consent form education

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this research is to understand whether schizophrenic patients are capable of comprehending clinical trial consent form or influenced by disease, also after intensified educational illustration for "understanding of consent form", their comprehension increased or not, in order to protect patient's right.

Full description

The goal of this research is to understand whether schizophrenic patients are capable of comprehending clinical trial consent form or influenced by disease, also after intensified educational illustration for "understanding of consent form", their comprehension will increase or not, in order to protect patient's right. First week, inform the patient a putative goal and method of clinical trial medicine research, then using Macarthur comprehension evaluation tool-clinical research Ed., evaluate the understanding of all patients for this putative clinical trial research consent form. For experimental group schizophrenic patients, using PANSS score evaluate seriousness of their symptom. 2 weeks later, randomly stratify schizophrenic patients into 2 groups, one give educational intervention for consent form, the other does not, then evaluate again with Macarthur comprehension evaluation tool-clinical research Ed. and PANSS score.

Enrollment

90 estimated patients

Sex

All

Ages

20 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Experimental group

  1. Age between 20 to 60, all genders.
  2. Psychiatry doctor diagnosed who met DSMIV-TR criteria schizophrenia.
  3. Participants require adequate ability to have a interview about 60-70min (include PANSS and Macarthur comprehension evaluation tool-clinical research Ed.).

Control group

  1. Age between 20 to 60, all genders.
  2. Psychiatry doctor diagnosed who exclude DSMIV-TR axis. I and II.
  3. Participants require adequate ability to have a interview about 30min (include PANSS and Macarthur comprehension evaluation tool-clinical research Ed.).

Exclusion criteria

Experimental group and control group

Participants have no adequate ability to have a interview about 60-70min (include PANSS and Macarthur comprehension evaluation tool-clinical research Ed.).

Trial design

90 participants in 2 patient groups

SchizoComp
Description:
Competence Ability of schizophrenia
Treatment:
Other: Consent form education
NonSchizoComp
Description:
Competence of Non-schizophrenia

Trial contacts and locations

1

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Central trial contact

Yuan-Feng Chang, MD.; Tsuo-Hung Lan, MD., PhD.

Data sourced from clinicaltrials.gov

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