A Study on the Preference of Risperidone Dosage Forms
1 other identifier
observational
1,000
1 country
1
Brief Summary
This study aimed to understand patients' needs and preferences for antipsychotic dosage forms.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 19, 2024
CompletedFirst Submitted
Initial submission to the registry
October 21, 2024
CompletedFirst Posted
Study publicly available on registry
October 24, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 28, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 28, 2025
CompletedOctober 24, 2024
September 1, 2024
5 months
October 21, 2024
October 23, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Proportion of patients (and their caregivers) who prefer risperidone patch-form medicine
The proportion of patients (and their caregivers) who preferred risperidone patch among the respondents in this study
"through study completion, an average of 6 months
Secondary Outcomes (1)
Factors related to patients' preference for risperidone patch-form medicines
through study completion, an average of 6 months
Study Arms (1)
Patients and their caregivers
Patients (and their caregivers) with psychiatric disorders for which risperidone is indicated, including schizophrenia, bipolar disorder, autism spectrum disorder, conduct disorder, and mental retardation.
Eligibility Criteria
Patients with schizophrenia, bipolar disorder, autism spectrum disorder, mental retardation or their primary caregivers who voluntarily participate in the study.
You may qualify if:
- Patients with schizophrenia, bipolar disorder, autism spectrum disorder, mental retardation or their primary caregivers who voluntarily participate in the study.
You may not qualify if:
- Have difficulty reading and understanding Chinese or refuse to participate in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Shanghai Mental Health Center
Shanghai, Shanghai Municipality, 200030, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 21, 2024
First Posted
October 24, 2024
Study Start
September 19, 2024
Primary Completion
February 28, 2025
Study Completion
February 28, 2025
Last Updated
October 24, 2024
Record last verified: 2024-09
Data Sharing
- IPD Sharing
- Will not share