About this trial
Schizophrenia represents a significant contributor to the global burden of disease, with this burden disproportionately impacting low- and middle-income countries (LMICs). In India, the burden due to schizophrenia is further exacerbated by low access to effective psychosocial interventions aimed at promoting recovery, rehabilitation, and community tenure, as well as inadequate attention to managing co-occurring chronic medical conditions that result in significantly reduced life expectancy among those living with schizophrenia compared to the general population. A major driver of these alarming gaps in access to care for persons with schizophrenia in India is the limited capacity within primary care settings aimed at addressing the complex co-occurring mental health, physical health, and functional needs of this patient population. There now exists strong evidence demonstrating that community programs delivered in primary care and leveraging psychosocial interventions combined with linkage to specialty psychiatric services are effective for supporting treatment and recovery of schizophrenia in low-resource settings. We will leverage our existing collaboration and robust research infrastructure in both rural and urban settings in Madhya Pradesh and Karnataka, India to conduct a hybrid type 1 effectiveness-implementation trial to evaluate whether the use of a digital platform offers added clinical benefit and can support integration of this task shared care for schizophrenia into routine primary care settings. We will address the following aims: 1) evaluate whether the use of the mindLAMP digital platform can enhance the clinical effectiveness of task-shared community-based psychosocial rehabilitation (COPSI) for individuals with schizophrenia, and 2) determine whether the addition of mindLAMP to the delivery of the COPSI program has an impact on implementation metrics when compared to delivery of COPSI alone.
Eligibility criteria
Qualifiers
Primary diagnosis of schizophrenia per IDC-10 diagnostic criteria for research and an illness duration of greater than 12 months and overall moderate level of severity on the CGI-SCH scale
At least one risk factor for early mortality (e.g. hypertension, diabetes, dyslipidemia, etc)
Willingness to stay in the study area during the trial period
Ability to operate a smartphone
Disqualifiers
Major visual impairment or inability to operate a smartphone
Cognitive impairment or diagnosis of dementia
Planning to move out of the study area in the next 12 months
Does not speak Hindi or Kannada
Trial design
Treatments tested in this trial
- Community care for People with Schizophrenia in India (COPSI)
- mindLAMP Mobile Application
Treatment groups
Locations
Sponsors and collaborators
Harvard Medical School (HMS and HSDM)
Lead sponsor
Beth Israel Deaconess Medical Center
Collaborator
Sangath
Collaborator
National Institute of Mental Health and Neuro Sciences, India
Collaborator
All India Institute of Medical Sciences, Bhopal
Collaborator