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A randomized controlled trial of Goal Management Training for executive functioning in schizophrenia spectrum disorders or psychosis risk syndromes.
Haugen, Ingvild; Stubberud, Jan; Haug, Elisabeth; McGurk, Susan R; Hovik, Kjell Tore; Ueland, Torill; Øie, Merete Glenne.
Affiliation
  • Haugen I; Division of Mental Health Care, Innlandet Hospital Trust, P. O. Box 104, 2381, Brumunddal, Norway. ingvild.haugen@sykehuset-innlandet.no.
  • Stubberud J; Department of Psychology, University of Oslo, P.O. Box 1094, 0317, Oslo, Norway. ingvild.haugen@sykehuset-innlandet.no.
  • Haug E; Department of Psychology, University of Oslo, P.O. Box 1094, 0317, Oslo, Norway.
  • McGurk SR; Department of Research, Lovisenberg Diaconal Hospital, P.O. Box 4970, Nydalen, 0440, Oslo, Norway.
  • Hovik KT; Division of Mental Health Care, Innlandet Hospital Trust, P. O. Box 104, 2381, Brumunddal, Norway.
  • Ueland T; Departments of Occupational Therapy and Psychological and Brain Sciences, Boston University, 930 Commonwealth Avenue, Boston, MA, 02215, USA.
  • Øie MG; Division of Mental Health Care, Innlandet Hospital Trust, P. O. Box 104, 2381, Brumunddal, Norway.
BMC Psychiatry ; 22(1): 575, 2022 08 28.
Article in En | MEDLINE | ID: mdl-36031616
ABSTRACT

BACKGROUND:

Executive functioning is essential to daily life and severely impaired in schizophrenia and psychosis risk syndromes. Goal Management Training (GMT) is a theoretically founded, empirically supported, metacognitive strategy training program designed to improve executive functioning.

METHODS:

A randomized controlled parallel group trial compared GMT with treatment as usual among 81 participants (GMT, n = 39 versus Wait List Controls, n = 42) recruited from an early intervention for psychosis setting. Computer generated random allocation was performed by someone independent from the study team and raters post-intervention were unaware of allocation. The primary objective was to assess the impact of GMT administered in small groups for 5 weeks on executive functioning. The secondary objective was to explore the potential of the intervention in influencing daily life functioning and clinical symptoms.

RESULTS:

GMT improved self-reported executive functioning, measured with the Behavior Rating Inventory of Executive Function - Adult version (BRIEF-A), significantly more than treatment as usual. A linear mixed model for repeated measures, including all partial data according to the principle of intention to treat, showed a significant group x time interaction effect assessed immediately after intervention (post-test) and 6 months after intervention (follow-up), F = 8.40, p .005, r .37. Improvement occurred in both groups in objective executive functioning as measured by neuropsychological tests, functional capacity, daily life functioning and symptoms of psychosis rated by clinicians. Self-reported clinical symptoms measured with the Symptoms Check List (SCL-10) improved significantly more after GMT than after treatment as usual, F = 5.78, p .019, r .29. Two participants withdrew due to strenuous testing and one due to adverse effects.

CONCLUSIONS:

GMT had clinically reliable and lasting effects on subjective executive function. The intervention is a valuable addition to available treatment with considerable gains at low cost. TRIAL REGISTRATION Registered at clinicaltrials.gov NCT03048695 09/02/2017.
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Full text: 1 Database: MEDLINE Main subject: Psychotic Disorders / Schizophrenia / Cognitive Behavioral Therapy Type of study: Clinical_trials / Etiology_studies / Risk_factors_studies Limits: Adult / Humans Language: En Year: 2022 Type: Article

Full text: 1 Database: MEDLINE Main subject: Psychotic Disorders / Schizophrenia / Cognitive Behavioral Therapy Type of study: Clinical_trials / Etiology_studies / Risk_factors_studies Limits: Adult / Humans Language: En Year: 2022 Type: Article