- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02283385
Mental Health Intervention for Elderly Abuse Victims (PROTECT)
Mental Health Intervention for Elderly Abuse Victims: Providing Options to Elderly Clients Together (PROTECT)
Study Overview
Detailed Description
Despite increasing recognition of the epidemic of elder abuse, we continue to face barriers helping abuse victims access and use elder abuse resolution services. In addition, many victims suffer from concurrent mental health problems that prevent them from taking the necessary steps to protect themselves. The proposed study will introduce a tailored intervention, built on an evidence-based approach (Problem Solving Therapy), to be delivered through a sustainable mental health program embedded in elder abuse services. The proposed psychotherapy is a brief 8-session weekly intervention that combines problem-solving therapy, anxiety management, and psycho education developed specifically for this population by this team.
The objectives of the project are to: identify the mental health needs of elder abuse victims, provide the mental health treatment, assess the impact of the treatment, and facilitate conditions which will sustain the mental health program.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
New York
-
New York, New York, United States, 10007
- Department for the Aging: Elderly Crime Victims Resource Center
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New York, New York, United States, 10018
- Jewish Association Serving the Aging
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Client of the New York City Department for the Aging's (DFTA) Elderly Crime Victims Resource Center
- Score of 10 or higher on the Patient Health Questionnaire (PHQ-9) or Generalized Anxiety Disorder 7-item scale (GAD-7)
Exclusion Criteria:
- Co-morbid psychiatric disorder other than unipolar non-psychotic major depression that prevents participation in depression and anxiety screening
- Inability to speak or understand English
- Cognitive impairment that prevents participation in screening, as determined by screening social worker
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: PROTECT Intervention
Participants will receive a brief psychotherapy that builds on Problem Solving Therapy (PST)
|
8-session weekly psychotherapy intervention that combines problem-solving therapy, anxiety management and psycho education developed specifically for this population
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Depression (Hamilton Depression Rating Scale)
Time Frame: 12 weeks
|
To document effectiveness of PROTECT intervention in reducing depressive symptoms.
Severity of depression will be assessed at baseline and 12 weeks using the Hamilton Depression Rating Scale as the primary measure.
|
12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Functioning (Behavioral Activation for Depression Scale)
Time Frame: 12 weeks
|
To document effectiveness of PROTECT intervention in increasing quality of life, social interaction, and overall functioning.
Severity will be assessed at baseline and 12 weeks using the Behavioral Activation for Depression Scale as the primary measure.
|
12 weeks
|
Service Utilization (specialized mistreatment and service outcome questionnaires)
Time Frame: 12 weeks
|
To document effectiveness of PROTECT intervention in increasing clients' utilization of elder abuse services and subsequently reporting a reduction in abuse.
Service utilization and severity of abuse will be assessed at baseline and 12 weeks using specialized mistreatment and service outcome questionnaires.
|
12 weeks
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Jo Anne Sirey, PhD, Weill Medical College of Cornell University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1306014011
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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