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Not yet recruiting NCT07157293

Online Intervention To Improve Motivation

No phase Interventional Schizophrenia Prodromal SCHIZOPHRENIA 1 (Disorder) Psychosis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Online Motivation Enhancing Intervention.
Who it may be relevant to
Registry conditions: Schizophrenia Prodromal, SCHIZOPHRENIA 1 (Disorder), Psychosis. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

An Online Intervention To Enhance Motivation and Goal-Directed Behavior

Overview

Participants will complete one online intervention lasting 12 weeks. Each week, they will be asked to complete a 20-30 minute session online. The intervention is targeting improved mood and positive affect in order to support increases in motivation and goal-directed behavior. Before and after the intervention, participants will be asked to complete measures to assess symptoms, mood, and behavior.

Interventions

  • Behavioral Online Motivation Enhancing Intervention
    This is a online intervention that will ask participants to review and complete 30 minutes of material each week.

Primary outcome measures

  • Brief Negative Symptom Scale [Time frame: immediately before and after the intervention]

Eligibility criteria

Inclusion criteria

  • Diagnosis of schizophrenia or a related psychotic disorder
  • Meeting criteria for being at clinical high risk for psychosis

Exclusion criteria

  • Does not have access to a computer each week

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

United States · 1 center
  • University of Alabama at Birmingham — Birmingham

Identifiers

NCT: NCT07157293 · 300015163 · Internal Award

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗