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Goals in Focus: CBT for Motivational Negative Symptoms of Psychosis (GIF)

U

University of Hamburg-Eppendorf

Status

Enrolling

Conditions

Schizophrenia
Psychosis
Negative Symptoms With Primary Psychotic Disorder

Treatments

Behavioral: Goals in Focus

Study type

Interventional

Funder types

Other

Identifiers

NCT05252039
DRKS00018083

Details and patient eligibility

About

This pilot feasibility trial aims to evaluate the "Goals in Focus" intervention for motivational negative symptoms in people with psychosis.

Goals in Focus interventions translate findings of basic clinical research on psychological mechanisms of motivational negative symptoms into a tailored and comprehensive novel psychological treatment program.

The current single-blind randomized-controlled study aims to test feasibility and to examine first estimates of the expected effect size of Goals in Focus to inform a subsequent fully-powered RCT.

The feasibility data will be used to improve on the trial design and the provision of the "Goals in Focus" intervention where necessary.

Full description

The reduction of goal-directed behavior is a core issue in motivational negative symptoms of psychosis and accounts for the long-term decline in psychological wellbeing and psychosocial functioning. However, the available treatment options are rather unspecific and show only small effects on motivational negative symptoms. Interventions that directly target the relevant psychological mechanisms of motivational negative symptoms are likely to be more effective. With "Goals in Focus", we translated findings of basic clinical research on psychological mechanisms of motivational negative symptoms into a tailored and comprehensive novel psychological treatment program for people with motivational negative symptoms. The current study aims to test the feasibility of Goals in Focus and trial procedures and 2) to estimate the expected effect size to inform a subsequent fully-powered trial.

A single-blind randomized-controlled trial will be conducted at the outpatient clinic of the Universität Hamburg, Germany. Thirty participants diagnosed with a psychotic spectrum disorder and at least moderate motivational negative symptoms will be randomly assigned to either 24 sessions of "Goals in Focus" or to a 6-months waitlist control group. Assessments will be conducted at baseline (t0) and 6 months after baseline completion (t1). Feasibility and acceptance of "Goals in Focus" will be rated by practitioners and participants. Feasibility of the trial procedures will be evaluated, e.g., with regard to patient recruitment, retention-, and attendance rates. The primary outcome for effect size estimation is defined as group differences in motivational negative symptoms at t1, corrected for baseline values. Secondary outcomes include psychosocial functioning, psychological well-being, depressive symptoms, expressive negative symptoms, negative symptom factors and goal-pursuit in everyday life.

The treatment effect on the primary outcomes will provide the basis for the sample size calculation for a fully powered RCT. The feasibility data will be used to improve on the trial design and the provision of the "Goals in Focus" intervention where necessary.

Enrollment

30 estimated patients

Sex

All

Ages

16 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ICD-10 diagnosis of a schizophrenia spectrum disorder (confirmed by the Structured Clinical Interview for DSM V Clinical Version
  • at least moderate motivational negative symptoms (i.e., scores ≥ 3 (moderate) in two items or ≥ 4 (moderately severe) in one item of the 'motivation and pleasure factor' of the Brief Negative Symptom Scale (BNSS)
  • sufficient skills in German language to participate in psychological therapy
  • capable to engage in weekly therapy sessions of 50-minutes
  • prioritize the reduction of negative symptoms as their current goal for treatment
  • capable to give informed consent to participate in the trial

Exclusion criteria

  • being at immediate and serious risk to self or others
  • co-morbid diagnosis of alcohol or substance use disorder
  • intake of Benzodiazepines for >2 days per week
  • receiving any other psychological treatment aiming to reduce motivational negative symptoms

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

Goals in Focus Therapy
Experimental group
Description:
Participants in this arm will receive 24 weekly sessions with Goals in Focus therapy (GiF) over 6 months.
Treatment:
Behavioral: Goals in Focus
Waitlist Control
No Intervention group
Description:
Participants in this arm will not receive any psychological treatment for 6 months. After 6-months, they will receive 24 sessions of Goals in Focus Therapy.

Trial contacts and locations

1

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Central trial contact

Matthias Pillny, Dr.

Data sourced from clinicaltrials.gov

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