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Mobile-Assisted Cognitive Behavior Therapy for Negative Symptoms in Schizophrenia

Mobile-Assisted Cognitive Behavior Therapy for Negative Symptoms in Schizophrenia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03179696
Acronym
mCBTn
Enrollment
31
Registered
2017-06-07
Start date
2016-08-15
Completion date
2018-10-31
Last updated
2024-11-08

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

Conditions

Schizoaffective Disorder, Schizophrenia

Keywords

Schizophrenia, CBSST, mobile CBT, negative symptoms

Brief summary

This clinical trial will test a combined group therapy plus mobile cognitive behavioral therapy intervention targeting defeatist attitudes in consumers with schizophrenia in order to change motivational negative symptoms linked to defeatist attitudes.

Detailed description

The primary purpose of this project is to test whether a psychosocial intervention, Cognitive Behavioral Social Skills Training (CBSST) combined with a smartphone-based cognitive-behavioral therapy for negative symptoms called, Mobile-assisted Cognitive Behavioral Therapy for Negative Symptoms (mCBTn) can reduce defeatist performance attitudes in consumers with schizophrenia spectrum disorders with persistent moderate-to-severe experiential negative symptoms.The project will also identify the optimal dose to engage the defeatist attitude target. Pupillary responses, an objective psychophysiological biomarker of effort, will be recorded during a cognitive task as a secondary outcome to determine its potential as an end point in clinical trials of motivation and effort.

Interventions

BEHAVIORALMobile-assisted CBT

mCBTn combines the CBT components that target defeatist attitudes from Cognitive Behavioral Social Skills Training (CBSST) group therapy and mobile smartphone interventions from our prior clinical trials research.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Eric Granholm
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* DSM-5 diagnosis of schizophrenia or schizoaffective disorder. * Meets prospective criteria for persistent moderate-to-severe experiential negative symptoms in at least two of the three CAINS Motivation and Pleasure domains (mean of 2 -moderate- or greater for items averaged within the Social, Work or Recreational domains) at the beginning and end of a 2-week evaluation phase. * Moderate-to-severe defeatist attitudes (DPAS \> 50). * ≥ 6th grade reading level on the Wide Range Achievement Test-4 Reading subtest (needed for reading treatment manual consumer workbook). * Clinically stable and stable on current medications (no changes within 3 months prior to enrollment and meeting all inclusion/

Exclusion criteria

during longitudinal baseline evaluation at both week -2 and 0).

Design outcomes

Primary

MeasureTime frameDescription
Defeatist performance beliefs (target mechanism)Assess change from baseline in defeatist performance beliefs at weeks 12, 18 and 24.Measure reduction of defeatist performance beliefs severity using the Defeatist Performance Attitude Scale.

Secondary

MeasureTime frameDescription
Pupillary responses as effort biomarkerAssess change from baseline in pupil dilation at week 12, 18 and 24.Measure changes in pupil dilation recorded during a digit span task.
Clinical Assessment Interview for Negative Symptoms (CAINS)Assess change from baseline in negative symptoms at week 12, 18 and 24.Measure changes in motivational negative symptoms on the CAINS.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026