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CompletedNCT02131116IMTUpdated Mar 29, 2018

Integrated Metacognitive Therapy in First Episode Psychosis

An interventional study of Integrated Metacognitive Therapy and Treatment as Usual in Schizophrenia, Schizophreniform Disorder and Schizoaffective Disorder, sponsored by Indiana University. Completed at 2 sites in United States. Open to participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2018-03-29.

Sponsored by Indiana University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

Insight, or lack of illness awareness, is a prominent and pressing clinical concern in the treatment and recovery of patients with psychotic disorders. Impaired insight results in poor treatment engagement and adherence, more frequent hospitalizations, greater positive and negative symptoms, and poor psychosocial functioning. Addressing these complications early in the disease process may lead to altered illness course with better outcomes. To date, only a small number of nonpharmacological interventions have been developed, none of which adequately address poor insight during the first few years of psychotic illness. Further, presently available therapeutic interventions do not attend to difficulties associated with improved insight, such as depression. The purpose of this investigation is to implement a novel intervention designed to improve insight, metacognition, neurocognition, symptoms, and ultimately overall functioning in persons with early psychosis. The novel intervention will integrate a number of previously established therapeutic approaches, such as metacognitive, narrative, cognitive behavioral and motivational interviewing, and hence be labeled Integrated Metacognitive Therapy (IMT). In order to measure the efficacy of IMT, all subjects will undergo a battery of assessments in each of these domains prior to and following either a novel intervention (N = 10) or treatment as usual (N = 10) for a period of approximately six months. Throughout the study, each IMT session (N = 10, 24 sessions each) will be audio recorded, transcribed, and de-identified to allow for careful ongoing qualitative analyses of potential active and inert ingredients of the approach and ultimately the development of an IMT manual which can then be tested in a larger, more rigorous randomized control trial. This investigation will play an important role in advancing current knowledge about treating insight in early psychosis. Further, it will serve to expand upon the intervention tools available by producing a much needed treatment manual designed specifically to target insight during an illness phase crucial for positive long term outcomes in psychosis.

Read the detailed description

The National Advisory Mental Health Council recently called for the development of non-pharmacological treatments that identify and target specific disease processes for clinical improvement in schizophrenia and other psychotic illnesses. One such illness process, vital for positive outcomes, is impaired awareness of illness or insight. Insight is often thought of as factual knowledge and acknowledgement of one's illness. More specifically, insight in psychosis has been conceptualized as a multi-dimensional construct, with several independent but overlapping dimensions, such as the ability to appropriately label aberrant mental events (e.g. hallucinations and delusions), recognition of illness, and willingness to engage in treatment. Relative to individuals with other mental illnesses, those with psychotic illness have the most impaired insight, presenting a number of challenges, including: poor treatment engagement and adherence, more frequent hospitalizations, greater positive and negative symptoms, and poor psychosocial functioning. This problem is particularly relevant in early phases of psychotic illness, where there remains a paucity of data. Data that is available has shown decreased insight is associated with increased symptoms and poorer cognitive functioning, both of which have the potential to impact illness course.

Two reasons account for a lack of attention to the development of treatments for insight: i) the lack of an adequate model of the forces which cause and sustain poor insight and ii) a failure to consider an integrated treatment. Without an idea of the processes which sustain poor insight, interventions have been able to offer education about the nature of illness but have not been equipped to respond to the underlying processes that block the emergence of insight in treatment. While earlier literature framed insight as a failure to grasp a specific fact, more recent efforts suggest poor insight is primarily the result of a failure to create a coherent account of the complex events and personal experiences related to a psychiatric illness. These difficulties becoming aware of one's illness may be multi-determined and result from factors including deficits in metacognition, neurocognition, and symptoms.

The development of insight is complex and highly dependent upon metacognitive processes, which have a unique, potentially moderating role. Metacognition involves a range of faculties that allow an individual to form representations of mental states of self and others, which then leads to the formation and revision of thoughts, beliefs, feelings, behaviors, and even individual aspirations. Therapies targeting metacognitive or mentalizing deficits have been successfully implemented for personality disorders, depression and anxiety. In psychotic disorders, decreased metacognitive capacity is thought to result in difficulties identifying the source of one's experiences, such as illness and its consequences. This leads to an inability to perceive the self as an active agent in the world and problems in understanding and acting upon the social cues (emotions and intentions) of others. A recently proposed Integrated Metacognitive therapeutic approach argues that insight will improve as an individual utilizes a constructed narrative to make sense of his or her experiences. In other words, illness and its consequences are understood in an individualized, personally relevant and acceptable way. Importantly, this approach addresses many obstacles to gaining insight not addressed by other approaches, including learning to deal with related emotional pain and depression, loss, and internalized stigma. This view is also consistent with intervention research showing that establishment of personal meaning is important for recovery, and promotes improved function and reduced symptoms. Case studies from our group and others have provided evidence that therapy targeting metacognitive processes is feasible in psychotic disorders and can indeed improve insight and function in persons with chronic schizophrenia. However, this approach has not been tailored to target insight, evaluated or tested in patients in the early phase of psychosis.

In addition to metacognitive deficits, neurocognitive deficits have also been commonly observed in schizophrenia and involve decrements in capacities for attention/vigilance, verbal memory and executive function. Deficits in executive function have been found to predict concurrent and prospective assessments of poorer insight, spurring hypotheses that impairments in executive function leave persons unable to synthesize illness related experiences into a coherent and adequate story about how and why they are ill. Deficits in attention and memory may additionally obscure how historical events are connected to each other. As a whole, neurocognitive deficits may cause difficulties piecing together the individual's experience of illness into a coherent whole resulting in poor insight. Therefore, development of personal narratives using an integrated therapy would allow subjects the opportunity to better understand their illness experience, hence improving insight.

The research presented above suggests that improving insight early in the psychotic disease process would likely result in improved treatment participation, ultimately leading to better outcomes. Motivated by a clear and pressing need to better address illness insight in early psychotic illness and recent positive findings related to doing so, the present investigation serves to test a novel Integrated Metacognitive Therapy (IMT) which targets insight and other important domains in early psychosis. Assuming IMT is successful, ongoing qualitative analysis of IMT sessions will allow for manual development, future randomized control trials, and ultimately treatment dissemination.

02

Conditions studied

  • Schizophrenia
  • Schizophreniform Disorder
  • Schizoaffective Disorder

Keywords

  • schizophrenia
  • schizophreniform disorder
  • schizoaffective disorder
  • cognition
  • metacognition
  • insight
  • first episode psychosis
  • psychosis
03

In context

Schizophrenia

3,472 studies on the registry are indexed under Schizophrenia; 472 are open to participants now.

This study's enrollment of 20 is below the median of 70 across 2,873 interventional studies indexed under Schizophrenia.

Browse Schizophrenia studies →

Lead sponsor

Indiana University is the lead sponsor of 958 studies on the registry; 200 are open to participants now.

Of its 142 completed or terminated interventional studies of FDA-regulated products, 112 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 18-35 years of age at study entry
  • Male or female
  • DSM IV-TR Diagnosis of schizophrenia, schizophreniform disorder, schizoaffective disorder as confirmed by Structured Clinical Interview for DSM-IV-TR (SCID)
  • Onset of schizophreniform disorder, schizophrenia, or schizoaffective disorder within the past five years as defined by first medical records documentation of these conditions
  • Score of 4 or higher (moderate impairment) on the Positive and Negative Syndrome Scale (PANSS) insight item

Exclusion criteria

Exclusion Criteria:

  • History of significant neurological illness or head trauma
  • Known IQ \< 70 based on medical history
  • Current alcohol or drug dependence (excluding nicotine or caffeine) based on the SCID interview.
  • Subjects considered a high risk for suicidal acts - active suicidal ideation as determined by clinical interview OR any suicide attempt in 90 days prior to screening
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    IMT

    Integrated Metacognitive Therapy

    Behavioral: Integrated Metacognitive Therapy · Behavioral: Treatment as Usual

  • No intervention
    TAU

    No intervention group/Treatment as Usual

Interventions

  • BehavioralIntegrated Metacognitive Therapy

    Integrated Metacognitive Therapy

  • BehavioralTreatment as Usual

    Treatment as Usual

    Also known as: No intervention/Treatment as Usual

06

What researchers measure

Primary outcomes

  1. Insight

    improved insight as measured by the Scale of Unawareness of Illness

    Time frame: 24 weeks

  2. Insight

    Insight item on the Positive and Negative Syndrome Scale

    Time frame: 24 weeks

  3. Insight

    Beck Cognitive Insight Scale

    Time frame: 24 weeks

  4. metacognition

    Bell Lysaker Emotion Recognition Test

    Time frame: 24 weeks

  5. metacognition

    scores on the the Eyes Test

    Time frame: 24 weeks

  6. metacognition

    scores on the Hinting Test

    Time frame: 24 weeks

  7. metacognition

    Indiana Psychiatric Illness Interview and Metacognitive Assessment Scale),

    Time frame: 24 weeks

Secondary outcomes

  1. overall symptomatology

    Positive and Negative Syndrome Scale

    Time frame: 24 weeks

  2. overall symptomatology

    Liebowitz Social Anxiety Scale

    Time frame: 24 weeks

  3. neurocognition

    Brief Assessment for Cognition in Schizophrenia total score

    Time frame: 24 weeks

  4. neurocognition

    Trail Making Test, Part B

    Time frame: 24 weeks

  5. social functioning

    Quality of Life Scale

    Time frame: 24 weeks

  6. social functioning

    Social Functioning Scale

    Time frame: 24 weeks

  7. social functioning

    Marlow-Crowne Social Desirability Scale

    Time frame: 24 weeks

07

Study locations

2 sites
  • Prevention and Recovery Center for Early Psychosis
    Indianapolis, Indiana 46202, United States
  • Psychosocial Rehabilitation and Recovery Center
    Indianapolis, Indiana 46202, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 29, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02131116
Lead sponsor
Indiana University
Responsible party
Jenifer Vohs (Clinical Psychologist, Indiana University) — Principal investigator
First posted
May 6, 2014
Start date
May 2014
Primary completion
Dec 2016
Completion
Dec 2017
Last update
Mar 29, 2018

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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