Alcohol Use Disorder Clinical Trial
— RESHAPE-cRCTOfficial title:
Reducing Stigma Among Healthcare Providers to Improve Mental Health Services: Cluster Randomized Controlled Trial (RESHAPE-cRCT)
A growing number of trials have demonstrated treatment effectiveness for mental illness by non-specialist providers, such as primary care providers, in low-resource settings. A barrier to scaling up these evidence-based practices is the limited uptake from trainings into service provision and lack of fidelity to evidence-based practices among non-specialists. This arises, in part, from stigma among non-specialists against people with mental illness. Therefore, interventions are needed to address attitudes among non- specialists. To address this gap, REducing Stigma among HeAlthcare Providers to improvE Mental Health services (RESHAPE), is an intervention for non-specialists in which social contact with persons with mental illness is added to training and supervision programs. A cluster randomized control trial will address primary objectives including changes in stigma (Social Distance Scale) and improved quality of mental health services, operationalized as accuracy of identifying patients with mental illness in primary care. The control condition is existing mental health training and supervision for non-specialists delivered through the Nepal Ministry of Health's adaptation of the World Health Organization mental health Gap Action Programme. The intervention condition will incorporate social contact with people with mental illness into existing training and supervision. Participants in the cluster randomized control trial will be the direct beneficiaries of training and supervision (primary care providers) and indirect beneficiaries (their patients). Primary care workers' outcomes include stigma (Social Distance Scale), knowledge (mental health Gap Action Programme knowledge scale), implicit attitudes (Implicit Association Test), clinical self-efficacy (mental health Gap Action Programme knowledge scale), and clinical competence (Enhancing Assessment of Common Therapeutic factors) to be assessed pre-training, post-training, and at 3- and 6-month follow-up. Accuracy of diagnoses will be determined through the Structured Clinical Interview for the Diagnostic and Statistical Manual version 5, which will be assessed at 3 months after patient enrollment. Patient outcomes include functioning, quality of life, psychiatric symptoms, medication side effects, barriers to care, and cost of care assessed at enrollment and 3 and 6 months. This study will inform decisions regarding inclusion of persons living with mental illness in training primary care providers.
Status | Recruiting |
Enrollment | 1300 |
Est. completion date | December 2024 |
Est. primary completion date | December 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 16 Years and older |
Eligibility | **Primary Care Providers** Inclusion Criteria: - All health workers from the facilities included in the study will be invited to participate - Health workers will be between 21 and 65 years of age based on employment criteria - within the government health system. - All participants will need to have Nepali language competency, - be actively engaged in care provision in their health cluster, - have a valid certificate of practice from the Ministry of Health - Health workers will need to have permission from their health supervisor to attend the entire duration of the training, Exclusion Criteria: - any prior citations on their clinical practice licensure or any other government credentialing violations. **Patients** Inclusion Criteria: - All patients (with non-emergency medical needs) presenting to the primary care - any of the following groups: - (a) any mental illness diagnosis including depression, psychosis (bipolar disorder with a manic episode, schizophrenia, major depressive disorder with psychotic features, and alcohol use disorder with psychosis) and alcohol use disorder; plus the other conditions included in Nepal's mental health Gap Action Programme: anxiety, conversion, epilepsy, dementia, child and adolescent, other substance abuse (these patients are included because misdiagnosis is common with regard to missing or overdiagnosing one condition in place of another mental illness); comorbid conditions are also acceptable; - (b) any patients screening above cut-off scores on the tools; and - (c) 10% of patients who are negative on all of the above criteria. - any patients previously treated for mental illness would be included - age range will be 16 years or older, with no upper age limit (mental health Gap Action Programme training covers child and adolescent through mental illnesses affecting elderly population). - all participants will be able to speak Nepali - able to complete the research interview with the research assistants who will read all of the assessment tools. Exclusion Criteria: - Patients with immediate medical needs requiring referral and emergency services (e.g., serious injury; pre-eclampsia; dehydration; status epilepticus) - patients needing acute psychiatric services (e.g., suicide attempts, alcohol withdrawal, psychosis/mania that cannot be managed in a community setting) who are referred for immediate hospitalization - Patients under the age of 16 years old will be excluded |
Country | Name | City | State |
---|---|---|---|
Nepal | Transcultural Psychosocial Organization Nepal | Pokhara | Province 4 |
Lead Sponsor | Collaborator |
---|---|
George Washington University | Duke University, King's College London, Transcultural Psychosocial Organization Nepal |
Nepal,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Social Distance Scale (SDS) | 12-item scale of willingness to interact with persons with mental illness, minimum = 0, maximum = 72, higher score is worse outcome | 6 months post training | |
Primary | Structured Clinical Interview for Diagnostic and Statistical Manual 5 (SCID-5) | Accuracy of clinical decision making (this a diagnostic tool, there are no maximum or minimum scores, the objective is to determine if an appropriate diagnosis is selected that will lead to appropriate management) | 3-months post-patient enrollment | |
Secondary | mental health Gap Action Programme knowledge test | Multiple-choice assessment from mental health Gap Action Programme training materials; minimum = 0, maximum = 100, higher is better outcome | 6 months post-training | |
Secondary | mental health Gap Action Programme knowledge test | Multiple-choice assessment from mental health Gap Action Programme training materials, minimum = 0, maximum = 100, higher is better outcome | 3 months post-training | |
Secondary | mental health Gap Action Programme knowledge test | Multiple-choice assessment from mental health Gap Action Programme training materials, minimum = 0, maximum = 100, higher is better outcome | immediately after the training | |
Secondary | mental health Gap Action Programme self-efficacy assessment | Self-reported clinical efficacy for mental health services, minimum = 0; maximum = 5, higher score is better outcome | 6-months post-training | |
Secondary | mental health Gap Action Programme self-efficacy assessment | Self-reported clinical efficacy for mental health services, minimum = 0; maximum = 5, higher score is better outcome | 3-months post-training | |
Secondary | mental health Gap Action Programme self-efficacy assessment | Self-reported clinical efficacy for mental health services, minimum = 0; maximum = 5, higher score is better outcome | immediately after the training | |
Secondary | Implicit Association Test | Computer-based neuropsychological assessment of implicit bias related to mental illness, there is no maximum or minimum score, score is D-score based on comparison of timing; positive scores equal more bias | 6-months post-training | |
Secondary | Implicit Association Test | Computer-based neuropsychological assessment of implicit bias related to mental illness, there is no maximum or minimum score, score is D-score based on comparison of timing; positive scores equal more bias | 3-months post-training | |
Secondary | Implicit Association Test | Computer-based neuropsychological assessment of implicit bias related to mental illness, there is no maximum or minimum score, score is D-score based on comparison of timing; positive scores equal more bias | immediately after the training | |
Secondary | Enhancing Assessment of Common Therapeutic factors | Observed structured clinical evaluation using a standardized role play, minimum score = 0, maximum = 100, higher scores are better | 6 months post-training | |
Secondary | Enhancing Assessment of Common Therapeutic factors | Observed structured clinical evaluation using a standardized role play, minimum score = 0, maximum = 100, higher scores are better | 3 months post-training | |
Secondary | Enhancing Assessment of Common Therapeutic factors | Observed structured clinical evaluation using a standardized role play, minimum score = 0, maximum = 100, higher scores are better | immediately after the training | |
Secondary | Social Distance Scale | 12-item scale of willingness to interact with persons with mental illness, minimum = 0, maximum = 72, higher score is worse outcome | 3 months post training | |
Secondary | Social Distance Scale | 12-item scale of willingness to interact with persons with mental illness, minimum = 0, maximum = 72, higher score is worse outcome | immediately after the training | |
Secondary | Patient: World Health Organization Disability Assessment Scale | Assessment of daily functioning, minimum = 12, maximum = 60; higher score is worse | 6-months post enrollment | |
Secondary | Patient: World Health Organization Disability Assessment Scale | Assessment of daily functioning, minimum = 12, maximum = 60; higher score is worse | 3-months post enrollment | |
Secondary | Patient Health Questionnaire 9 | Depression symptoms, minimum = 0, maximum = 27, higher score is worse | 6-months post enrollment | |
Secondary | Patient Health Questionnaire 9 | Depression symptoms, minimum = 0, maximum = 27, higher score is worse | 3-months post enrollment | |
Secondary | Patient: Generalized Anxiety Disorder 7 | Anxiety symptoms, minimum = 0, maximum = 21, higher score is worse | 6 months post enrollment | |
Secondary | Patient: Generalized Anxiety Disorder 7 | Anxiety symptoms, minimum = 0, maximum = 21, higher score is worse | 3 months post enrollment | |
Secondary | Patient: Positive and Negative Symptoms of Schizophrenia | Psychosis symptoms, minimum = 0, maximum = 56, higher score is worse | 6 months post enrollment | |
Secondary | Patient: Positive and Negative Symptoms of Schizophrenia | Psychosis symptoms, minimum = 0, maximum = 56, higher score is worse | 3 months post enrollment | |
Secondary | Patient: Alcohol Use Disorder Identification Test | Alcohol Use Disorder symptoms, minimum = 0, maximum = 40, higher score is worse | 6-months post enrollment | |
Secondary | Patient: Alcohol Use Disorder Identification Test | Alcohol Use Disorder symptoms, minimum = 0, maximum = 40, higher score is worse | 3-months post enrollment | |
Secondary | Patient: Euroqol 5 dimension 5 level | Quality of life symptoms, minimum = 5, maximum=25, higher score is worse | 6-months post enrollment | |
Secondary | Patient: Euroqol 5 dimension 5 level | Quality of life symptoms, minimum = 5, maximum=25, higher score is worse | 3-months post enrollment | |
Secondary | Patient: Cost of Service Receipt Inventory | Costs of care to patients, there is no maximum or minimum score, the outcome is total costs | 6-months post-enrollment | |
Secondary | Patient: Cost of Service Receipt Inventory | Costs of care to patients, , there is no maximum or minimum score, the outcome is total costs | 3-months post-enrollment | |
Secondary | Patient: Enhancing Assessment of Common Therapeutic factors | Common factors use by primary care provider, minimum score = 0, maximum = 15, higher score is better | 6-months post-enrollment |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04788004 -
Long-term Recovery: Longitudinal Study of Neuro-behavioral Markers of Recovery and Precipitants of Relapse
|
||
Recruiting |
NCT05684094 -
Mechanisms of Risky Alcohol Use in Young Adults: Linking Sleep to Reward- and Stress-Related Brain Function
|
N/A | |
Completed |
NCT03406039 -
Testing the Efficacy of an Online Integrated Treatment for Comorbid Alcohol Misuse and Emotional Problems
|
N/A | |
Completed |
NCT03573167 -
Mobile Phone-Based Motivational Interviewing in Kenya
|
N/A | |
Completed |
NCT04817410 -
ED Initiated Oral Naltrexone for AUD
|
Phase 1 | |
Active, not recruiting |
NCT04267692 -
Harm Reduction Talking Circles for American Indians and Alaska Natives With Alcohol Use Disorders
|
N/A | |
Completed |
NCT03872128 -
The Role of Neuroactive Steroids in Stress, Alcohol Craving and Alcohol Use in Alcohol Use Disorders
|
Phase 1 | |
Completed |
NCT02989662 -
INIA Stress and Chronic Alcohol Interactions: Glucocorticoid Antagonists in Heavy Drinkers
|
Phase 1/Phase 2 | |
Recruiting |
NCT06030154 -
Amplification of Positivity for Alcohol Use
|
N/A | |
Active, not recruiting |
NCT05419128 -
Family-focused vs. Drinker-focused Smartphone Interventions to Reduce Drinking-related Consequences of COVID-19
|
N/A | |
Completed |
NCT04564807 -
Testing an Online Insomnia Intervention
|
N/A | |
Completed |
NCT04284813 -
Families With Substance Use and Psychosis: A Pilot Study
|
N/A | |
Completed |
NCT04203966 -
Mental Health and Well-being of People Who Seek Help From Their Member of Parliament
|
||
Recruiting |
NCT05861843 -
Craving Assessment in Patients With Alcohol Use Disorder Using Virtual Reality Exposure
|
||
Terminated |
NCT04404712 -
FAAH Availability in Psychiatric Disorders: A PET Study
|
Early Phase 1 | |
Enrolling by invitation |
NCT04128761 -
Decreasing the Temporal Window in Individuals With Alcohol Use Disorder
|
N/A | |
Not yet recruiting |
NCT06337721 -
Preventing Alcohol Use Disorders and Alcohol-Related Harms in Pacific Islander Young Adults
|
N/A | |
Not yet recruiting |
NCT06163651 -
Evaluating a One-Year Version of the Parent-Child Assistance Program
|
N/A | |
Not yet recruiting |
NCT06444243 -
Psilocybin-assisted Therapy for Alcohol Use Disorder
|
Phase 2 | |
Enrolling by invitation |
NCT02544581 -
Preliminary Analysis of the Soberlink Alcohol Breath Analyzer System's (SABA) Clinical Utility During Aftercare
|
N/A |