search
Back to results

Decision-making and Decision Support Among Emerging Adults With First Episode Psychosis

Primary Purpose

Early Psychosis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Decision aid
Sponsored by
Temple University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Early Psychosis

Eligibility Criteria

18 Years - 25 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Aged 18 to 25 years
  • Experiencing early psychosis, defined as psychosis lasting 18 months or less between the time when threshold symptom criteria were reached (as determined by the admitting CSC program assessor) and the date of CSC program enrollment
  • Planning to attend a medication appointment with a participating CSC psychiatrist
  • Ability to speak and understand English
  • Ability to provide informed consent as assessed by research staff using procedures discussed by Carpenter et al. (2000) including a demonstrated understanding and recall of study procedures, rather than passive consent, and allowance of repetition of study procedures until there is understanding and recall.

Exclusion Criteria:

  • Have a legal guardian
  • Have identified co-occurring dementia, delirium, or intellectual disability that will likely affect their ability to provide informed consent or participate in the data collection procedures.

Sites / Locations

  • Psychosis Education, Assessment, Care and Empowerment (PEACE)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Decision aid (DA)

Treatment as usual (TAU)

Arm Description

a one-page DA for use during the psychiatric consultation to help patients and clinicians discuss relevant treatment options pertaining to antipsychotics.

Treatment as usual without the DA

Outcomes

Primary Outcome Measures

Change in antipsychotics knowledge
Scale to assess change in knowledge about antipsychotic medications over time (9 items)
Decision-making self-efficacy
Decision Self-Efficacy (DSE) scale to assess decision self-efficacy (11 items)
Decision-making attitudes
Decision Attitude Scale (DAS) to assess decision-making attitudes (10 items)
Decisional Conflict
Decisional Conflict Scale (DCS) to assess level of decisional conflict (15 items)
Shared decision making
collaboRATE scale to assess level of shared decision making after an appointment (3 items)
Change in medication adherence
Brief Adherence Rating Scale (BARS) to assess change in medication adherence over time (8 items)
Change in service use
Service Use and Resource Form for Monthly Items (SURF-M) scale to assess change in service use over time (66 items)
Service engagement
Service Engagement Scale (SES) to assess level of service engagement (14 items)

Secondary Outcome Measures

Apathy
Marin Apathy Evaluation Scale to assess apathy (18 items)
Attachment style
Experiences in Close Relationships-Revised (ECR-R) Questionnaire to assess attachment style (36 items)
Working alliance
Working Alliance Inventory (WAI) to assess alliance (36)
Trust
Trust in the Medical Profession Scale to assess level of trust in the clinician (11 items)
Cognitive functioning
Brief Assessment of Cognition in Schizophrenia (BACS) - a battery to assess aspects of cognition such as verbal memory and attention.
Insight
Birchwood Insight Scale to assess insight to the illness (8 items)
Self-stigma
Internalized Stigma of Mental Illness (ISMI) Scale - Brief Version, to assess mental health self-stigma (10 items)

Full Information

First Posted
April 29, 2020
Last Updated
February 12, 2021
Sponsor
Temple University
search

1. Study Identification

Unique Protocol Identification Number
NCT04373590
Brief Title
Decision-making and Decision Support Among Emerging Adults With First Episode Psychosis
Official Title
Mental Healthcare Decision-Making and Decision Support Among Emerging Adults Enrolled in Coordinated Specialty Care for Early Psychosis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
February 27, 2019 (Actual)
Primary Completion Date
August 12, 2020 (Actual)
Study Completion Date
August 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Temple University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the impact of an antipsychotic medication decision aid and interpersonal and cognitive factors, such as attachment style and motivation, on emerging adults' ability to engage in shared decision making regarding their medications.
Detailed Description
The long-term occupational, social, and economic outcomes associated with psychosis make it an urgent public health problem. Coordinated specialty care (CSC) is now the gold standard for early psychosis, demonstrating positive clinical and functional effects in the short-term, and longer-term reduced hospitalization rates. These services include an array of treatment options, including psychotropic medications, individual psychotherapy, family education, and support, and occupational therapy and supported employment/education. While a shorter period between psychosis onset and receipt of appropriate care is associated with better outcomes, emerging adults often experience significant delays before receiving treatment, and a large percentage disengage from services once they are commenced. Decisional conflict about treatment options (i.e., feeling conflicted about which option to choose) and interpersonal factors such as attachment style and trust in health providers can contribute to decision delay and discontinuance of chosen options. Decision support tools (e.g., decision aids), have been shown to reduce decisional conflict as well as improve service engagement. A requisite step in expanding the array of decision support tools available to emerging adults experiencing early psychosis is to better understand their decision-making ability, capacity, and motivation to engage in decision making and how these relate to their engagement in CSC. It is well recognized that individuals who are being prescribed antipsychotic medications often face decisional conflict about their treatment options. An especially controversial decision is whether individuals should continue taking medication at the same dose or adjust the dose whilst monitoring their symptoms. This dilemma is the result of some uncertainty about the appropriate treatment strategy for long-term management of psychosis. The present project focuses on evaluating the feasibility and effectiveness of the use of a decision aid for making decisions about antipsychotic medication.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Early Psychosis

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Masking Description
Randomization is accomplished using a HIPAA-compliant, Internet-based randomization service (studyrandomizer.com) using permuted blocks of 5. Patients and the participating psychiatrist are not blinded to the condition assigned to them; however, they are not given any explicit information on the DA. The psychiatrist was provided with the DA and received information about it as the DA is delivered by the psychiatrist for patients who are randomized to receive it. The RA who recruit and administer assessments to participants is not blinded to condition, except at baseline.
Allocation
Randomized
Enrollment
18 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Decision aid (DA)
Arm Type
Experimental
Arm Description
a one-page DA for use during the psychiatric consultation to help patients and clinicians discuss relevant treatment options pertaining to antipsychotics.
Arm Title
Treatment as usual (TAU)
Arm Type
No Intervention
Arm Description
Treatment as usual without the DA
Intervention Type
Behavioral
Intervention Name(s)
Decision aid
Intervention Description
The chosen intervention is a one-page DA developed by the first author, published and fully described elsewhere (Zisman-Ilani et al., 2017; Zisman et al., 2018) for use during the psychiatric consultation to help patients and clinicians discuss relevant treatment options pertaining to antipsychotics such as medication nonadherence and self-tapering. The DA format is a simple one-page table with rows containing frequently asked questions by patients about their treatment options and the benefits, risks, and implications of differing decisions. The columns display the treatment options available for the treatment decision in question: continuing, adjusting, or discontinuing antipsychotic medications.
Primary Outcome Measure Information:
Title
Change in antipsychotics knowledge
Description
Scale to assess change in knowledge about antipsychotic medications over time (9 items)
Time Frame
Baseline (Pre-appointment interview ) and post appointment interview ( same 1 day of the appointment )
Title
Decision-making self-efficacy
Description
Decision Self-Efficacy (DSE) scale to assess decision self-efficacy (11 items)
Time Frame
Post appointment interview (1 day of the appointment )
Title
Decision-making attitudes
Description
Decision Attitude Scale (DAS) to assess decision-making attitudes (10 items)
Time Frame
Post appointment interview (1 day of the appointment )
Title
Decisional Conflict
Description
Decisional Conflict Scale (DCS) to assess level of decisional conflict (15 items)
Time Frame
Post appointment interview (1 day of the appointment )
Title
Shared decision making
Description
collaboRATE scale to assess level of shared decision making after an appointment (3 items)
Time Frame
Post appointment interview (1 day of the appointment )
Title
Change in medication adherence
Description
Brief Adherence Rating Scale (BARS) to assess change in medication adherence over time (8 items)
Time Frame
Baseline (Pre-appointment interview ) and post appointment interview ( same 1 day of the appointment ), 3 months follow-up , 6 months follow-up .
Title
Change in service use
Description
Service Use and Resource Form for Monthly Items (SURF-M) scale to assess change in service use over time (66 items)
Time Frame
Baseline (Pre-appointment interview ) and post appointment interview ( same 1 day of the appointment ), 3 months follow-up , 6 months follow-up .
Title
Service engagement
Description
Service Engagement Scale (SES) to assess level of service engagement (14 items)
Time Frame
Baseline (Pre-appointment interview )
Secondary Outcome Measure Information:
Title
Apathy
Description
Marin Apathy Evaluation Scale to assess apathy (18 items)
Time Frame
Baseline (Pre-appointment interview )
Title
Attachment style
Description
Experiences in Close Relationships-Revised (ECR-R) Questionnaire to assess attachment style (36 items)
Time Frame
Baseline (Pre-appointment interview )
Title
Working alliance
Description
Working Alliance Inventory (WAI) to assess alliance (36)
Time Frame
Baseline (Pre-appointment interview )
Title
Trust
Description
Trust in the Medical Profession Scale to assess level of trust in the clinician (11 items)
Time Frame
Baseline (Pre-appointment interview )
Title
Cognitive functioning
Description
Brief Assessment of Cognition in Schizophrenia (BACS) - a battery to assess aspects of cognition such as verbal memory and attention.
Time Frame
Baseline (Pre-appointment interview )
Title
Insight
Description
Birchwood Insight Scale to assess insight to the illness (8 items)
Time Frame
Baseline (Pre-appointment interview )
Title
Self-stigma
Description
Internalized Stigma of Mental Illness (ISMI) Scale - Brief Version, to assess mental health self-stigma (10 items)
Time Frame
Baseline (Pre-appointment interview )

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Aged 18 to 25 years Experiencing early psychosis, defined as psychosis lasting 18 months or less between the time when threshold symptom criteria were reached (as determined by the admitting CSC program assessor) and the date of CSC program enrollment Planning to attend a medication appointment with a participating CSC psychiatrist Ability to speak and understand English Ability to provide informed consent as assessed by research staff using procedures discussed by Carpenter et al. (2000) including a demonstrated understanding and recall of study procedures, rather than passive consent, and allowance of repetition of study procedures until there is understanding and recall. Exclusion Criteria: Have a legal guardian Have identified co-occurring dementia, delirium, or intellectual disability that will likely affect their ability to provide informed consent or participate in the data collection procedures.
Facility Information:
Facility Name
Psychosis Education, Assessment, Care and Empowerment (PEACE)
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19123
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29788933
Citation
Zisman-Ilani Y, Shern D, Deegan P, Kreyenbuhl J, Dixon L, Drake R, Torrey W, Mishra M, Gorbenko K, Elwyn G. Continue, adjust, or stop antipsychotic medication: developing and user testing an encounter decision aid for people with first-episode and long-term psychosis. BMC Psychiatry. 2018 May 22;18(1):142. doi: 10.1186/s12888-018-1707-x.
Results Reference
result
PubMed Identifier
33431018
Citation
Zisman-Ilani Y, Hurford I, Bowen A, Salzer M, Thomas EC. Evaluating the feasibility of a decision aid to promote shared decision making among young adults with first-episode psychosis: protocol for a pilot study. Pilot Feasibility Stud. 2021 Jan 11;7(1):22. doi: 10.1186/s40814-020-00757-0.
Results Reference
derived

Learn more about this trial

Decision-making and Decision Support Among Emerging Adults With First Episode Psychosis

We'll reach out to this number within 24 hrs