Skip to content

The Consta Club: A Demonstration Project for Setting up a Consta Club in a Community Mental Health Center

The Consta Club: A Demonstration Project for Setting up a Consta Club in a Community Mental Health Center

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00845572
Enrollment
30
Registered
2009-02-18
Start date
2007-01-31
Completion date
2010-06-30
Last updated
2012-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizoaffective, Schizophrenia

Keywords

Schizophrenia, Schizoaffective, Risperdal Consta, Medication Adherence, Antipsychotic

Brief summary

This study will establish a bi-weekly Consta Club. Participants will begin taking Risperdal Consta after being recommended by their treating physician. As a part of the Consta Club attendees will receive their injection of Risperdal Consta and be educated about important mental health issues. Interviews with study participants will be completed every three months to determine the effectiveness of the change to Risperdal Consta and the bi-weekly group. The overall hypothesis is that the individuals in Consta Club will have a decrease in walk-in visits, emergency procedures and hospitalizations. It is also believed that individuals in Consta Club will have fewer symptoms and better levels of functioning.

Detailed description

Poor adherence to oral antipsychotic medication leads to rehospitalization, derails the process of recovery, and contributes to the high cost of treating schizophrenia. Unfortunately, poor adherence is common for individuals with this diagnosis. An organizing hypothesis of our research program is that forgetfulness and failure to establish a routine that facilitates medication adherence are prominent reasons for non-adherence. We have established a thirty minute bi-weekly Consta Club in which individuals will attend a social group and and also receive their injection of Risperdal Consta. Consta Club will educate individuals about the importance of medication adherence as well as establish a routine that facilitates adherence. The club will provide the opportunity for the club members to discuss their mental illness, develop goals to recovery, establish a means of transportation to the club and participate in drawings to win prizes. The overall hypothesis is that the individuals in Consta Club will experience a decrease in walk-in visits, emergency procedures and hospitalizations. It is also hypothesized that individuals in Consta Club will demonstrate lower levels of symptomatology, higher levels of quality of life and improvements in functioning when compared to their baseline. A total of twenty-five individuals will be recruited to switch from an oral atypical antipsychotic medication to Risperdal Consta which will be supplied by Janssen Pharmaceutica at no cost to the individual or the clinic. Individuals will be recruited prior to hospital discharge if inpatient at time of recruitment OR from the local mental health clinic. Hospitalized individuals will be started on Risperdal Consta prior to discharge and outpatients will switch from oral atypical antipsychotics within two weeks. Individuals will be receiving a single injection of Risperdal Consta every two weeks. Prior to the switch and every 3 months for a period of 9 months the individual will be assessed.

Interventions

BEHAVIORALConsta Club

Biweekly group for patients receiving Risperdal Consta injections. Each 45 minute group includes socialization time, goal-setting, illness and medication education, and refreshments.

Sponsors

Ortho-McNeil Janssen Scientific Affairs, LLC
CollaboratorINDUSTRY
The University of Texas Health Science Center at San Antonio
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Males and females who are able to understand the consent form and who have given informed consent. 2. Between the ages of 18 and 65. 3. Diagnosis of schizophrenia or schizoaffective disorder 4. Receiving treatment with an oral atypical antipsychotic medication for at least two months prior to study 5. Only partial adherence (80% or less) to antipsychotic medication 6. If they have tried Consta but did not receive an adequate trial and did not experience any adverse symptoms. 7. Some responsibility for attending Consta Club meetings and injections. 8. Able to understand and complete rating scales.

Exclusion criteria

1. History of significant head trauma, seizure disorder, or mental retardation. 2. Has a legal guardian. 3. Alcohol or drug abuse or dependence within the past 3 months. 4. Previous negative reactions to oral Risperdal.

Design outcomes

Primary

MeasureTime frame
Service Utilization - Patients in consta club will have fewer missed visits, fewer unscheduled visits, and fewer emergency visits and hospitalizations than matched patients on oral antipsychoticsend of study

Secondary

MeasureTime frame
Patients in consta club will demonstrate lower levels of symptomatology and higher levels of quality of life and community adjustment than matched patients on oral antipsychoticsend of study

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026