Status:

COMPLETED

In-person vs. Remote Wellness Support

Lead Sponsor:

The University of Texas Health Science Center at San Antonio

Collaborating Sponsors:

National Institute of Mental Health (NIMH)

Conditions:

Depressive Disorder, Major

Bipolar Disorder

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

The study team will use components of the Reach, Effectiveness, Adoption, Implementation, Maintenance (RE-AIM) framework to compare Cognitive Adaptation Training (CAT) to Remotely delivered Cognitive ...

Detailed Description

Individuals choosing or assigned to R-CAT will continue treatment as usual with their health care team and R-CAT will be added. R-CAT is a remotely delivered version of CAT focused on medication adher...

Eligibility Criteria

Inclusion

  • Able to give informed consent.
  • Between the ages of 18 and 65.
  • Clinical Diagnosis of Major Depressive Disorder, Bipolar disorder, Schizophrenia, or Schizoaffective Disorder
  • Receiving treatment with oral psychiatric medications.
  • Have had a hospitalization or emergency department visit in the past year
  • Have a Medication Possession Ratio (MPR) based upon electronic refill data below 80% at least 1 of the past 4 quarters with at least 1 psychiatric medication
  • Responsible for taking their own medications
  • Report on telephone prescreen call with researcher team that they have missed at least 2 doses of medication in the past 3 weeks, that they are willing to take medication and would like remote assistance to take medication more regularly
  • Report on telephone prescreen call with research team that they have 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
  • Report on prescreen research call with research team that they have no plans to change their MCO in the next 12 months
  • Have a working smart phone
  • Able to understand and complete rating scales and assessments.
  • Agree to home visits for intervention and to count pills and conduct assessments

Exclusion

  • Substance dependence within the past 2 months
  • Currently being treated by an ACT team
  • Documented history of violence or threatening behavior on initial assessment
  • Receive home visits to assist with medication adherence
  • Unable to complete baseline assessments

Key Trial Info

Start Date :

November 24 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 11 2022

Estimated Enrollment :

56 Patients enrolled

Trial Details

Trial ID

NCT04526067

Start Date

November 24 2020

End Date

November 11 2022

Last Update

September 5 2024

Active Locations (1)

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University of Texas Health Science Center - Department of Psychiatry

San Antonio, Texas, United States, 78229