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Evaluation of the Achieving Depression and Anxiety Patient Centered Treatment (ADAPT) Program

Evaluating the Implementation and Outcomes of the Achieving Depression and Anxiety Patient Centered Treatment (ADAPT) Collaborative Care Program in A Large, Integrated Healthcare System: A Mixed Methods Observational Study Protocol

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04839718
Acronym
ADAPT
Enrollment
0
Registered
2021-04-09
Start date
2019-04-01
Completion date
2022-12-31
Last updated
2023-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression

Keywords

Depression, Anxiety

Brief summary

Depression and anxiety are increasingly common conditions for which primary care providers (PCPs) serve as the initial healthcare contact for most patients. Comorbid depression and anxiety result in higher costs, and treatment as usual, which is referrals to specialty psychiatric care, often contribute to delays in care. Collaborative psychiatric care is an evidence-based strategy to increase mental healthcare access while reducing costs. ADAPT is a novel collaborative care model. By using technology-driven appointments with providers, ADAPT increases access to mental healthcare, and reduces member wait times. This mixed methods study will assess implementation measures of the ADAPT program and the components of ADAPT related to patient mental health improvement compared to specialty mental health care. The hypothesis is that: ADAPT program will have good program reach and efficacy. We will examine program implementation and maintenance. Further, the study looks to uncover member and program characteristics that are associated with depression and anxiety remission and care utilization.

Interventions

BEHAVIORALADAPT

The Achieving Depression and Anxiety Patient Centered Treatment (ADAPT) Program is a novel collaborative psychiatric care model that is designed to unburden PCPs and psychiatrists, increase access to quality specialty mental healthcare for Kaiser Permanente members, and improve patient depression and anxiety treatment outcomes by utilizing technology-driven appointments. This program uses principles of collaborative care, including patient-centered care, population-based care, evidence-based care, measurement-based treatment to target, and accountable care.

Sponsors

Kaiser Permanente
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Adult Outcomes Questionnaire (AOQ) score between 10-30 * English-Speaking

Exclusion criteria

* High risk for suicide defined by answer to question 9 on PHQ-9 of 1 or more * Diagnosis of bipolar disorder * Diagnosis of a psychotic disorder * Dementia diagnosis * Active substance use disorder diagnosis * Current hospice * Current home-based palliative care * Residing in a skilled nursing facility * Residing in an assisted living facility * Non-Kaiser Permanente Member * Established psychiatric care outside of Kaiser Permanente

Design outcomes

Primary

MeasureTime frameDescription
Patient reachthrough study completion, 2 yearsExamine and compare patients eligible and enrolled in ADAPT versus those eligible but not enrolled in ADAPT

Secondary

MeasureTime frameDescription
Member characteristics associated with depression remissionbaseline, 3 and 6 monthsClinical variables important to predicting intervention response: Patient demographics (age, sex, race/ethnicity, socioeconomic status), behavioral characteristics (exercise, sleep), and other individual characteristics (comorbidities, adverse childhood experiences, social supports, resilience).
Member characteristics associated with anxiety remissionbaseline, 3 and 6 monthsClinical variables important to predicting intervention response: Patient demographics (age, sex, race/ethnicity, socioeconomic status), behavioral characteristics (exercise, sleep), and other individual characteristics (comorbidities, adverse childhood experiences, social supports, resilience).
Efficacy: Patient therapy engagementbaseline, 3 and 6 monthsnumber of therapy contacts (individual, group and combined)
Efficacy: Patient medication provider engagementbaseline, 3 and 6 monthsnumber of clinical pharmacy contacts
Efficacy: Patient psychiatry engagementbaseline, 3 and 6 monthsnumber of contact with psychiatrist
Efficacy: Patient time to carebaseline, 3 and 6 monthsaverage time from ADAPT referral to first appointment with therapist or pharmacist
Efficacy: Patient medication engagementbaseline, 3 and 6 monthsmedication length of treatment
Efficacy: Anxiety outcomesbaseline, 3 and 6 monthsExamine if patients enrolled in ADAPT demonstrate non-inferior anxiety outcomes defined by generalized anxiety disorder (GAD-2) score compared to treatment as usual.
Efficacy: Time to clinical improvementbaseline, 3 and 6 monthsCompare time to clinical improvement as defined by change in Adult Outcomes Questionnaire (AOQ score) from baseline to 3, and 6 months for members in ADAPT compared to treatment as usual.
Implementation: measurement-based carethrough study completion, 2 yearsExamine provider use of measurement-based care
Implementation: Diagnosisthrough study completion, 2 yearsExamine provider use of a specific depression or anxiety diagnosis
Maintenance: Measurement-based carethrough study completion, 2 yearsExamine provider use of measurement-based care over time
Maintenance: Diagnosisthrough study completion, 2 yearsExamine provider use of a specific depression or anxiety diagnosis over time
Efficacy: Depression outcomesbaseline, 3 and 6 monthsExamine if patients enrolled in ADAPT demonstrate non-inferior depression outcomes defined by change in the patient health questionnaire (PHQ-9) score compared to treatment as usual.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026