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

Primary Purpose

Psychosis, Schizophrenia, Negative Symptoms With Primary Psychotic Disorder

Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Goals in Focus
Sponsored by
University of Hamburg-Eppendorf
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Psychosis focused on measuring Amotivation, Avolition, Anhedonia, Asociality

Eligibility Criteria

16 Years - 85 Years (Child, Adult, Older Adult)All SexesDoes not accept 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

Sites / Locations

  • Psychotherapeutische Hoschschulambulanz Universität HamburgRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Goals in Focus Therapy

Waitlist Control

Arm Description

Participants in this arm will receive 24 weekly sessions with Goals in Focus therapy (GiF) over 6 months.

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.

Outcomes

Primary Outcome Measures

Brief Negative Symptoms Scale (BNSS) - 'motivation and pleasure factor' score
The primary outcome is defined as the change in motivational negative symptoms assessed with the 'motivation and pleasure factor' of the Brief Negative Symptoms Scale (BNSS). The BNSS is a 13-item semi-structured interview measuring negative symptoms on two factors, namely 'motivation and pleasure' and 'reduced expressivity'. The 'motivation and pleasure factor' includes seven items that measure the subscales of 'anhedonia', 'avolition', and 'asociality'. Symptoms are rated on a seven-point scale ranging from 0 "no impairment" to 6 "severe deficit"

Secondary Outcome Measures

Avolition, Asociality and Anhedonia
The respective subscales of the Brief Negative Symptom Scale according to the five-factor model. Each scale ranges from 0 to 6 with higher scores indicating higher symptom severity
Role Functioning Scale (RFS)
Psychosocial Functioning across different domains of social roles
Global Assessment of Functioning (GAF)
Observer-rating of psychosocial functioning. Ranges from 0 to 100 with higher scores indicating better functioning
Warwick-Edinburgh Mental Well-Being Scale (WEMWBS)
Self-reported psychological well-being. Scores range from 14 to 70 with higher scores indicating higher well-being
Calgary Depression Rating Scale for Schizophrenia (CDSS)
Semi-structured interview ti assess depressive symptoms. Scores range from 0 to 36 with higher scores indicating more depressive symptoms
Goal-pursuit within daily-life
Daily-life goal-pursuit will be assessed using the Experience Sampling Method (ESM). Participants will be prompted two times per day (10am and 10pm) over the course of one week via the MovisensXSapplication (Movisens GmbH) installed on a smartphone device. At the beginning of the ESM assessment, the participants' self-efficacy will be assessed with the Generalized Self-Efficacy Scale (GSE) Each of the following '10am prompts' will ask the participants to nominate a goal that they would like to achieve during the respective day and to rate characteristics of this goal (e.g., goal-commitment, goal-importance, goal-difficulty etc.). At the '10pm prompts', participants will be asked to indicate to what extent they achieved the respective goal and to answer questions on their causal-attributions and affective experience regarding their goal-achievement.

Full Information

First Posted
January 28, 2022
Last Updated
May 8, 2023
Sponsor
University of Hamburg-Eppendorf
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1. Study Identification

Unique Protocol Identification Number
NCT05252039
Brief Title
Goals in Focus: CBT for Motivational Negative Symptoms of Psychosis
Acronym
GIF
Official Title
Goals in Focus: CBT for Motivational Negative Symptoms of Psychosis - a Randomized-controlled Feasibility Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2020 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Hamburg-Eppendorf

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psychosis, Schizophrenia, Negative Symptoms With Primary Psychotic Disorder
Keywords
Amotivation, Avolition, Anhedonia, Asociality

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
prospective, randomized, controlled, parallel-group, two-armed
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Goals in Focus Therapy
Arm Type
Experimental
Arm Description
Participants in this arm will receive 24 weekly sessions with Goals in Focus therapy (GiF) over 6 months.
Arm Title
Waitlist Control
Arm Type
No Intervention
Arm 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.
Intervention Type
Behavioral
Intervention Name(s)
Goals in Focus
Intervention Description
Goals in Focus (GiF) is a symptom-specific treatment program that targets motivational negative symptoms in patients with schizophrenia-spectrum disorders. The aim is to improve setting and pursuit of personal relevant goals. GiF follows a 24-individual-sessions treatment manual. GiF includes five treatment phases: 1) Preparation, 2) Goal-setting, 3) Goal-pursuit, and 4) Reflection and preparation of autonomous goal-pursuit. The interventions include generating positive goals, behavioral activation, training of anticipatory pleasure, challenging demotivating beliefs, training of problem-solving skills and social skills training.
Primary Outcome Measure Information:
Title
Brief Negative Symptoms Scale (BNSS) - 'motivation and pleasure factor' score
Description
The primary outcome is defined as the change in motivational negative symptoms assessed with the 'motivation and pleasure factor' of the Brief Negative Symptoms Scale (BNSS). The BNSS is a 13-item semi-structured interview measuring negative symptoms on two factors, namely 'motivation and pleasure' and 'reduced expressivity'. The 'motivation and pleasure factor' includes seven items that measure the subscales of 'anhedonia', 'avolition', and 'asociality'. Symptoms are rated on a seven-point scale ranging from 0 "no impairment" to 6 "severe deficit"
Time Frame
6 months after baseline assessment
Secondary Outcome Measure Information:
Title
Avolition, Asociality and Anhedonia
Description
The respective subscales of the Brief Negative Symptom Scale according to the five-factor model. Each scale ranges from 0 to 6 with higher scores indicating higher symptom severity
Time Frame
6 months after baseline assessment
Title
Role Functioning Scale (RFS)
Description
Psychosocial Functioning across different domains of social roles
Time Frame
6 months after baseline assessment
Title
Global Assessment of Functioning (GAF)
Description
Observer-rating of psychosocial functioning. Ranges from 0 to 100 with higher scores indicating better functioning
Time Frame
6 months after baseline assessment
Title
Warwick-Edinburgh Mental Well-Being Scale (WEMWBS)
Description
Self-reported psychological well-being. Scores range from 14 to 70 with higher scores indicating higher well-being
Time Frame
6 months after baseline assessment
Title
Calgary Depression Rating Scale for Schizophrenia (CDSS)
Description
Semi-structured interview ti assess depressive symptoms. Scores range from 0 to 36 with higher scores indicating more depressive symptoms
Time Frame
6 months after baseline assessment
Title
Goal-pursuit within daily-life
Description
Daily-life goal-pursuit will be assessed using the Experience Sampling Method (ESM). Participants will be prompted two times per day (10am and 10pm) over the course of one week via the MovisensXSapplication (Movisens GmbH) installed on a smartphone device. At the beginning of the ESM assessment, the participants' self-efficacy will be assessed with the Generalized Self-Efficacy Scale (GSE) Each of the following '10am prompts' will ask the participants to nominate a goal that they would like to achieve during the respective day and to rate characteristics of this goal (e.g., goal-commitment, goal-importance, goal-difficulty etc.). At the '10pm prompts', participants will be asked to indicate to what extent they achieved the respective goal and to answer questions on their causal-attributions and affective experience regarding their goal-achievement.
Time Frame
6 months after baseline assessment
Other Pre-specified Outcome Measures:
Title
Feasibility referrals
Description
number of referrals (number of participants referred to the study)
Time Frame
throughout the trial; approximately two years after recruitment commenced
Title
Feasibility participant eligibility
Description
eligibility rates (proportion of enrolled participants found eligible)
Time Frame
throughout the trial; approximately two years after recruitment commenced
Title
Feasibility consents
Description
number of participants consenting to study participation and reasons for refusals
Time Frame
throughout the trial; approximately two years after recruitment commenced
Title
Feasibility retention
Description
retention rate (i.e., number and proportion of participants who attend t1 assessment and completeness of data at t1)
Time Frame
throughout the trial; approximately two years after recruitment commenced
Title
Feasibility adherence
Description
attendance rates and dose of intervention (i.e., number of sessions delivered within six months)
Time Frame
throughout the trial; approximately two years after recruitment commenced
Title
Feasibility data attrition
Description
data attrition (proportion of outcome data not obtained)
Time Frame
throughout the trial; approximately two years after recruitment commenced
Title
Acceptability participants
Description
- drop-out rate (i.e., number of withdrawals)
Time Frame
throughout the trial; approximately two years after recruitment commenced
Title
Acceptability and trial safety
Description
- number of adverse and serious adverse events that are considered adverse reactions to the intervention
Time Frame
throughout the trial; approximately two years after recruitment commenced
Title
Treatment satisfaction participants
Description
- participant satisfaction with treatment and personal outcomes (post-intervention questionnaire)
Time Frame
throughout the trial; approximately two years after recruitment commenced
Title
Treatment satisfaction therapists
Description
- therapist satisfaction (post-intervention questionnaire therapist version)
Time Frame
throughout the trial; approximately two years after recruitment commenced

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Matthias Pillny, Dr.
Phone
+4940428384023
Email
matthias.pillny@uni-hamburg.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tania M Lincoln, Prof. Dr.
Organizational Affiliation
Universität Hamburg
Official's Role
Principal Investigator
Facility Information:
Facility Name
Psychotherapeutische Hoschschulambulanz Universität Hamburg
City
Hamburg
ZIP/Postal Code
20146
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne K Fladung, Dr.
Email
anne.fladung@uni-hamburg.de
First Name & Middle Initial & Last Name & Degree
Tania M Lincoln, Prof. Dr.

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
only upon request

Learn more about this trial

Goals in Focus: CBT for Motivational Negative Symptoms of Psychosis

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