NCT06657430

Brief Summary

This study aimed to understand patients' needs and preferences for antipsychotic dosage forms.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Sep 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 19, 2024

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

October 21, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 24, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2025

Completed
Last Updated

October 24, 2024

Status Verified

September 1, 2024

Enrollment Period

5 months

First QC Date

October 21, 2024

Last Update Submit

October 23, 2024

Conditions

Keywords

risperidonepatchcross-sectional studypreference

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

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

RECRUITING

MeSH Terms

Conditions

SchizophreniaBipolar DisorderAutism Spectrum DisorderConduct DisorderIntellectual Disability

Condition Hierarchy (Ancestors)

Schizophrenia Spectrum and Other Psychotic DisordersMental DisordersBipolar and Related DisordersMood DisordersChild Development Disorders, PervasiveNeurodevelopmental DisordersAttention Deficit and Disruptive Behavior DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Lan Luo, Doctor of Medicine

CONTACT

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

Locations