Enhancing Motivation in Recent Onset Schizophrenia (PRIME)

University of California San Francisco (UCSF)

Status: Terminated

Conditions: Schizophrenia

Treatments: Behavioral: PRIME; Behavioral: Cognitive Training

Study type: Interventional

Funder types: Other

Identifiers

NCT01817387

NIMHK23SCH

Details and patient eligibility

About

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.

Enrollment: 20 patients

Sex: All

Ages: 14 to 30 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Factorial Assignment

Masking: Single Blind

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20 participants in 2 patient groups

PRIME + CT

Experimental group

Description:

4 months use of PRIME mobile application on mobile device and 30 hours of cognitive training

Treatment:

Behavioral: Cognitive Training

Behavioral: PRIME

Daily Goals + CT

Experimental group

Description:

4 months use of Daily Goals mobile application on mobile device and 30 hours of cognitive training

Treatment:

Behavioral: Cognitive Training