Cognitive Adaption Training-Effectiveness in Real-world Settings and Mechanism of Action (CAT-EM)

Sponsor
The University of Texas Health Science Center at San Antonio (Other)
Overall Status
Recruiting
CT.gov ID
NCT03829280
Collaborator
Vanguard Research Group (Other), National Institute of Mental Health (NIMH) (NIH)
500
8
2
75.9
62.5
0.8

Study Details

Study Description

Brief Summary

The investigators propose a cluster randomized effectiveness trial comparing Cognitive Adaptation Training (CAT; a psychosocial treatment using environmental supports such as signs, alarms, pill containers, checklists, technology and the organization of belongings established in a person's home or work environment to bypass the cognitive and motivational difficulties associated with schizophrenia ) to existing community treatment (CT) for individuals with schizophrenia in 8 community mental health centers across multiple states including 400 participants. Mechanisms of action will be examined. Participants will be assessed at baseline and 6 and 12 months on measures of functional and community outcome, medication adherence, symptoms, habit formation and automaticity, cognition and motivation.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Cognitive Adaptation Training
  • Behavioral: Community Treatment
N/A

Detailed Description

Schizophrenia remains one of the most disabling conditions world-wide with an economic burden that exceeded $155 billion dollars in fiscal year 2013 alone. Despite existing medication and community treatment, many individuals with this diagnosis continue to have poor outcomes and struggle toward recovery. CAT is a psychosocial treatment using environmental supports such as signs, alarms, pill containers, checklists, technology and the organization of belongings established in a person's home or work environment to bypass the cognitive and motivational difficulties associated with schizophrenia, and support habits for functional behavior to promote recovery. In a series of efficacy studies, CAT improved social and occupational functioning, symptoms, and adherence to medication, and reduced rates of readmission. The investigators propose a cluster randomized effectiveness trial comparing Cognitive Adaptation Training (CAT) to existing community treatment (CT) for individuals with schizophrenia in 8 community mental health centers across multiple states including 400 participants. This would be the first large-scale effectiveness study of CAT for improving functional outcomes for those with schizophrenia seen in community mental health centers (CMHCs) where the majority of those with schizophrenia are followed for outpatient care and to study the purported mechanisms of action based on an integrated theoretical model. Participants will be assessed at baseline and 6 and 12 months on measures of functional and community outcome, medication adherence, symptoms, habit formation and automaticity, cognition and motivation. CAT treatment will be weekly for 6 months, biweekly for 3 months and monthly for the remainder of the trial. Purported mechanisms of action for CAT including bypassing impairments in cognitive function to improve functional outcome and bypassing motivational impairments to create automatic habits to improve functional outcome will be examined.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Cluster Randomized clinical trial conducted at 8 community mental health outpatient treatment sites across the countryCluster Randomized clinical trial conducted at 8 community mental health outpatient treatment sites across the country
Masking:
Single (Outcomes Assessor)
Masking Description:
Raters assessing clinical outcome variables are centralized raters who are blind to treatment group as well as study design and aims.
Primary Purpose:
Treatment
Official Title:
Cognitive Adaption Training-Effectiveness in Real-world Settings and Mechanism of Action (CAT-EM)
Actual Study Start Date :
Apr 4, 2019
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Aug 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Cognitive Adaptation Training

Psychosocial treatment using environmental supports such as signs, alarms, pill containers, checklists, technology and the organization of belongings established in a person's home or work environment to bypass the cognitive and motivational difficulties associated with schizophrenia, and support habits for functional behavior to promote recovery.

Behavioral: Cognitive Adaptation Training
Psychosocial treatment using environmental supports to bypass cognitive and motivational problems and improve adaptive behavior
Other Names:
  • CAT
  • Active Comparator: Community Treatment

    Medication follow-up and case management as provided by the community mental health center according to usual care.

    Behavioral: Community Treatment
    Medication follow-up and case management as provided in usual community care in the setting
    Other Names:
  • CT
  • Outcome Measures

    Primary Outcome Measures

    1. Change in Social and Occupational Functioning Scale Scores [baseline, 6 months, 12 months]

      A rating from 0-100 reflecting global level of Social and Occupational functioning; Higher scores indicate better functioning.

    Secondary Outcome Measures

    1. Change in Daily activity [baseline, 6 months, 12 months]

      Negative Symptom Assessment item 14 assessing typical daily behavior using a structured interview with behavioral anchor points. Scale is rated 1 to 6 with higher scores indicating lower levels of engagement in daily activity (i.e. more severe apathy)

    2. Change in Multnomah Community Ability Scale mean score [baseline, 6 months, 12 months]

      Assessment of community functioning on a 17 -item scale with domains assessing interference with functioning, adjustment to living, social competence and behavioral problems. Items are averaged to produce a mean score. Items are each rated on a scale from 1-5 with higher scores reflecting better community functioning.

    3. Change in Adherence Estimate Score [baseline, 6 months, 12 months]

      A 3 item scale assessing variables associated with adherence. Items are rated based upon self report about the importance of taking medication, worry about medication and financial burden of medication on a scale from agree completely to disagree completely. Each answer is assigned points based on an algorithm and added producing a total score. Higher scores indicate a higher risk for adherence and a lower probability of adherence. Scores range for 0 to 100.

    4. Change in Negative Symptom Assessment-16 Mean Score [baseline, 6 months, 12 months]

      Assesses 16 negative symptoms in the domains of communication, emotion/affect, social activity, motivation and psychomotor activity on a scale from 1-6. Items are added and divided by 16 to produce a mean score. A global score is also produced based upon clinical judgement following the interview Higher scores reflect higher levels of negative symptoms.

    5. Change in the Expanded Version Brief Psychiatric Rating Scale (BPRS)-total score [baseline, 6 months, 12 months]

      24 item scale assessing multiple dimensions of psychopathology including positive symptoms; negative symptoms, anxiety/depression, and activation on a series of 7 point scales. Higher scores reflect higher levels of symptoms.

    Other Outcome Measures

    1. Change in Effort Expenditure for Rewards Task (EEfRT) Probability Difference score [baseline, 6 months, 12 months]

      computerized task of effort put forth to win various amounts of money under various levels of probability. The probability difference score equals the percent of hard choices in the high probability condition minus the percent of hard choices in the low probability condition. Higher scores indicate more frequent choices of hard tasks at the high versus low probability level. individuals who answer the same way on all tasks are eliminated (estimate 1%)

    2. Change in global score of Brief Assessment of Cognition (BACS) App [baseline, 6 months, 12 months]

      Ipad delivered version of BACS assessing memory, attention, executive function and psychomotor speed. Standard scores are generated and summed to create a global cognition score with higher scores indicating better levels of cognitive function.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Males and females who have given informed consent.

    2. Between the ages of 18 and 65.

    3. Clinical Diagnosis of Schizophrenia, or Schizoaffective Disorder

    4. Able to provide evidence of a stable living environment (individual apartment, family home, board and care facility) within the last three months and no plans to move in the next year.

    5. Able to understand and complete rating scales and assessments.

    6. Agree to home visits

    7. Be able to have reimbursed home visits as part of treatment

    Exclusion Criteria:
    1. Alcohol or drug or dependence within the past 2 months.

    2. Currently being treated by an Assertive Community Treatment (ACT) team.

    3. History of assault within the past year or other conditions that in the judgement of the treatment team make home visits unsafe.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 United Services Inc. Dayville Connecticut United States 06241
    2 Henderson Behavioral Health Lauderdale Lakes Florida United States 33319
    3 Chestnut Health Systems Granite City Illinois United States 62040
    4 Community Mental Health Center Inc. Lawrenceburg Indiana United States 47025
    5 Mental Health Center of Greater Manchester Manchester New Hampshire United States 03101
    6 Peace Health Eugene Oregon United States 97401
    7 Providence Center Providence Rhode Island United States 02904
    8 The Harris Center for Mental Health & IDD Houston Texas United States 77074

    Sponsors and Collaborators

    • The University of Texas Health Science Center at San Antonio
    • Vanguard Research Group
    • National Institute of Mental Health (NIMH)

    Investigators

    • Principal Investigator: Dawn Velligan, PhD, University of Texas

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    The University of Texas Health Science Center at San Antonio
    ClinicalTrials.gov Identifier:
    NCT03829280
    Other Study ID Numbers:
    • HSC20180237H
    • 1R01MH117101-01
    First Posted:
    Feb 4, 2019
    Last Update Posted:
    Jun 21, 2022
    Last Verified:
    Jun 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by The University of Texas Health Science Center at San Antonio
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 21, 2022