- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04704362
Ensuring Quality in Psychological Support (EQUIP)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
There is increasing evidence that non-specialist or minimally trained mental health providers can effectively provide support and deliver psychosocial support and low-intensity psychological interventions for common mental disorders and substance use disorders in low resource settings. Psychological treatments delivered by non-specialists in low-resource settings have effectiveness comparable to high-income country studies of specialist interventions.
Low intensity interventions refer to interventions that do not rely on specialists and are modified, brief evidence-based therapies including guide self-help and e-mental health. The World Health Organization identifies such interventions as being: brief, basic, non-specialist-delivered versions of existing evidence-based psychological treatments (e.g., basic versions of cognitive-behavioral therapy, interpersonal therapy); and may include self-help materials (e.g., self-help books, audiovisual materials, and online or app-based self-help interventions); individual or group programs, and designed to be age-appropriate (i.e., delivered differently for children and adults). Moreover, low intensity interventions are particularly well suited to communities affected by adversity, as they use fewer resources which make them more scalable.
Psychosocial refers to interventions that are designed to address the psychological effects of conflict [or adversity], including the effects on behavior, emotion, thoughts, memory and functioning, and social effects, including changes in relationships, social support and economic status. The term psychosocial emphasizes, the close connection between psychological aspects of experience and wider social aspects of experience, inclusive of human capacity, social ecology, and culture and values. For the purpose of this study, low intensity psychological and psychosocial interventions were selected using the criteria above, and ensuring the interventions are freely accessible to the public.
To assure success of such interventions outside the context of resource-intensive research trials, it is crucial to develop training and supervision programs that produce competent providers of psychological and psychosocial support interventions. A necessary element to achieve this goal is development of standardized tools and procedures to assess the competency of those trained to deliver them; while ensuring competency assessment results are easily understandable to trainers and supervisors so that they can remediate areas of low competency.
In the context of psychological and psychosocial interventions, competency refers the extent to which a therapist [including non-specialists] has the knowledge and skill required to deliver a treatment to the standard needed for it to achieve its expected effects. Competency is typically assessed through structured role-plays in which trained standardized [mock] clients elicit trainee's ability to perform the key skills of an intervention. Role-plays such as this are commonly used in health professional training and evaluation in the form of observed structured clinical evaluations with simulated patients. The Ensuring Quality in Psychological Support initiative was developed out of need to have easily implementable competency evaluation tools and remediation training materials that can be used with specialists and non-specialists in diverse global settings. To supplement the platform, Ensuring Quality in Psychological Support will also include various implementation, trainer and training resources and guidance.
The need for these competency assessment tools and training materials was identified in May 2018, during a Theory of Change Workshop conducted by the World Health Organization Ensuring Quality in Psychological Support team with frontline psychological service practitioners, clinicians, non-governmental organization training and supervision staff, and researchers. The four key elements of the platform will be (a) competency tools for evaluation of non-specific (core competencies or common factors) and specific practice elements (or treatment specific factors); (b) role-play vignettes for conducting competency evaluations; (c) instructional materials on how to conduct competency evaluations (training standardized clients, establishing inter-rater reliability when conducting competency evaluations, using rating tools, interpreting results); and (d) instructional materials on how to integrate competency evaluations into trainings and supervision (giving feedback to participants, modifying training programs, feedback to trainers and supervisors) including core competency training and remediation materials.
Study Goals and Objectives:
The goal of the study is to inform development of the Ensuring Quality in Psychological Support platform and its tools, ensuring feasibility, acceptability, utility, reliability, and validity to support the provision of quality psychological support.
Study Objectives
- Determine the feasibility, acceptability, and perceived utility, of the Ensuring Quality in Psychological Support platform to facilitate assessment of competency and employ competency assessment results and remediation training materials to support training and supervision of non-specialists on low-intensity psychological interventions.
- Evaluate the reliability, validity, and sensitivity to change of Ensuring Quality in Psychological Support competency assessment tools based on inter-rater reliability of the tools within and between sites, ability to detect changes in competency over the course of training and supervision, and association with trainer ratings, as well as service delivery metrics and client outcomes across different psychological interventions and implementation sites.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Addis Ababa, Ethiopia
- Center for Victims of Torture
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Amman, Jordan
- Institute for Family Health
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Nairobi, Kenya
- University of Nairobi
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Beirut, Lebanon
- War Child Holland
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Lince, Peru, 15046
- Socios En Salud Sucursal Peru
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Kampala, Uganda
- HealthRight International Uganda
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Lusaka, Zambia, 10101
- Centre for Infectious Disease Research in Zambia
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Trainees: Non-specialist in mental health and psychosocial support
- Clients: Site-specific level of distress to determine psychological intervention participation
Exclusion Criteria:
- Trainees: Unable to comprehend language that training and supervision will be conducted in
- Clients: Serious mental illness, developmental disability
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: TRIPLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
ACTIVE_COMPARATOR: Training and Supervision as Usual
Non-specialists are trained in a psychological intervention under standard conditions.
No feedback from competency-based evaluations is provided to modify the training or supervision curriculum.
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Trainees are trained using a manual for non-specialist-delivered psychological interventions.
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EXPERIMENTAL: Competency-based Training and Supervision
Non-specialists are trained and supervised in a competency-based approach in which trainers and/or supervisors are provided with the competency scores of trainees in order to modify the training and supervision content and approach as needed.
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Trainees are evaluated with the Enhancing Assessment of Common Therapeutic factors structured role play tool and the results are shared with trainers and/or supervisors to modify training based on strengths and weakness on the competency scores.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Trainee - Enhancing Assessment of Common Therapeutic factors; Unabbreviated scale title: "Enhancing Assessment of Common Therapeutic Factors"
Time Frame: Post-intensive supervision (approximately 1 month post-training)
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15-item objective structured clinical examination using a role play, minimum value = 15, maximum value = 60, higher score means greater competency
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Post-intensive supervision (approximately 1 month post-training)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Trainee - Enhancing Assessment of Common Therapeutic factors; Unabbreviated scale title: "Enhancing Assessment of Common Therapeutic Factors"
Time Frame: immediately after the manualized psychological treatment training
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15-item objective structured clinical examination using a role play, minimum value = 15, maximum value = 60, higher score means greater competency
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immediately after the manualized psychological treatment training
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Trainee - Trainer Subjective Rating of Competency; unabbrievated scale title "Trainer Subjective Rating of Competency"
Time Frame: immediately after the manualized psychological treatment training
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Trainer's subjective competency rating of trainee on a scale from 1 to 4, with higher scores reflecting greater competency.
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immediately after the manualized psychological treatment training
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Trainer's subjective competency rating of trainee on a scale from 1 to 4, with higher scores reflecting greater competency.
Time Frame: Post-intensive supervision (approximately 1 month post-training)
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Trainer's subjective competency rating of trainee on a scale from 1 to 4, with higher scores reflecting greater competency.
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Post-intensive supervision (approximately 1 month post-training)
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Trainee - Equip-Treatment-specific competencies; unabbreviated title "Ensuring Quality in Psychological Support Treatment Specific Competency"
Time Frame: Immediate post-training (last day of training on manualized intervention)
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Site specific measure of trainee's competencies in manualized psychological intervention delivered by non-specialists; mean scores range from 1=potentially harmful, 2=some basic skills; 3=all basic skills; 4=advanced skills; higher score is more competency
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Immediate post-training (last day of training on manualized intervention)
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Trainee - Equip-Treatment-specific competencies; unabbreviated title "Ensuring Quality in Psychological Support Treatment Specific Competency"
Time Frame: Post-intensive supervision (approximately 1 month post-training)
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Site specific measure of trainee's competencies in manualized psychological intervention delivered by non-specialists; mean scores range from 1=potentially harmful, 2=some basic skills; 3=all basic skills; 4=advanced skills; higher score is more competency
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Post-intensive supervision (approximately 1 month post-training)
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Client - mental health outcome, for example, Patient Health Questionnaire; unabbreviated title "Patient Health Questionnaire"
Time Frame: Immediately after completion of the manualized psychological treatment
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Site specific mental health outcome measure of client; higher scores reflect greater psychological distress; for example, Patient Health questionnaire range from 0 to 27; greater score is more symptoms.
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Immediately after completion of the manualized psychological treatment
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Client - functioning outcome, for example, unabbreviated title: "World Health Organization Disability Assessment Schedule"
Time Frame: Immediately after completion of the manualized psychological treatment
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Site specific client functional impairment measure; higher scores reflect greater functional impairment; for example, World Health Organization Disability Assessment Schedule score range from 0 to 60; greater score is more impairment.
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Immediately after completion of the manualized psychological treatment
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Alison Schafer, PhD, World Health Organization
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 (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NCR191797
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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