Triple Aim Psychotherapy: Aimed at Improving Patient Experience, Population Health, and Cost
NCT03659591 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80
Last updated 2018-09-06
Summary
Community mental health programs in publically-funded jurisdictions such as Canada often have limited budgets in order to provide services, which can result in inadequate access to effective treatment for patients. Cognitive Behaviour Therapy (CBT) is a gold-standard psychotherapy for depression and anxiety. In order to improve access to treatment, community mental healthcare settings often provide CBT in a group format for patients experiencing mild-to-moderate symptoms. However, typical protocols for delivering group CBT in a community setting nonetheless require a considerable investment of limited clinician time. The Institute for Healthcare Improvement (IHI) developed the Triple Aim, which is a framework describing an approach to optimizing health system performance by simultaneously pursuing three dimensions, namely improving the patient experience of care; improving the health of populations; and reducing the associated per capita costs of care. Adaptive Psychological Training (APT) is a group-based psychotherapy designed with all of the dimensions of the Triple Aim in mind simultaneously. In its development, APT drew heavily upon mindfulness-based approaches. To-date, APT has already demonstrated positive outcomes in pilot research and in community clinical settings. The purpose of the current study is to determine whether for a given population of patients experiencing mild-to-moderate symptoms of depression and/or anxiety, APT can facilitate meaningful change for more patients per time spent by clinicians than can CBT.
Conditions
- Anxiety Symptoms
- Depressive Symptoms
Interventions
- BEHAVIORAL
-
Cognitive Behaviour Therapy
CBT will be delivered in group format, consisting of 10 weekly two-hour sessions, with 10 participants per group
- BEHAVIORAL
-
Adaptive Psychological Training
APT will be delivered in group format, consisting of 5 weekly two-hour sessions, with 20 participants per group
Sponsors & Collaborators
-
Joseph Brant Hospital
lead OTHER
Principal Investigators
-
Steven Selchen, MD MSt FRCPC · Joseph Brant Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-09-30
- Primary Completion
- 2019-08-31
- Completion
- 2019-11-30
Countries
- Canada
Study Locations
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