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Enhancing Motivation in Recent Onset Schizophrenia

Developing an Intervention Strategy to Enhance Motivation in Recent Onset Schizophrenia

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01817387
Acronym
PRIME
Enrollment
20
Registered
2013-03-25
Start date
2014-07-31
Completion date
2018-03-20
Last updated
2020-01-23

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

Conditions

Schizophrenia

Brief summary

This project will result in the development of a personalized intervention strategy to improve motivation for treatment engagement and functional outcomes in individuals with a recent onset of schizophrenia. Motivational impairment is arguably the single most important factor that determines a patient's ability to engage in and adhere to effective treatment. In our study, sixty participants will be enrolled in a randomized controlled trial comparing the feasibility and tolerability of two types of motivational interventions (Daily Goals or PRIME), and a neuroplasticity-based cognitive training program. Participants are randomized to either receive Daily Goals or PRIME for 8 weeks, after which, both conditions will also receive an 8-week course of cognitive training delivered via iPads. Participants will undergo pre/post-testing and a 6-month follow-up to determine feasibility and efficacy of the interventions. By enhancing motivation, schizophrenia patients would be able to engage more fully with treatment and develop full and productive lives. This study may also pave the way forward for other health conditions in which motivational impairments impede health outcomes. All assessments will be conducted at the University of California, San Francisco; however, we offer some assessments to be done remotely.

Interventions

BEHAVIORALPRIME

Mobile application designed to improve psychosocial functioning and motivational deficits

BEHAVIORALCognitive Training

Auditory processing, verbal learning, memory, processing speed, and social cognition

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
14 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of schizophrenia, schizoaffective, or schizophreniform disorder. * Onset of diagnosis within 5 years. * 14-30 years old. * Clinically stable (outpatient status for 1 month and stable dose of medication for 1 month). * Good general health

Exclusion criteria

* Substance dependence within the past 12 months, * Current substance abuse, * No history of neurological disorder

Design outcomes

Primary

MeasureTime frameDescription
Psychosocial functioningpast 30 daysWork status, work performance, social status, social performance, health status, health performance

Countries

United States

Outcome results

None listed

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