Individual Placement and Support and/or Cognitive Remediation Therapy Added to TAU in Patients With Early Schizophrenia
Primary Purpose
Schizophrenia, Schizophreniform Disorders, Schizoaffective Disorder
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Individual Placement and Support
Cognitive Remediation Therapy
Sponsored by
About this trial
This is an interventional treatment trial for Schizophrenia
Eligibility Criteria
Inclusion Criteria:
- Male/Female patients aged between 18-35 years.
- Diagnosis of schizophrenia confirmed by SCID meeting DSM-V criteria for schizophrenia, schizophreniform or schizoaffective psychosis.
- Stable on medication for the past four weeks.
- In contact with mental health services
- Within 5 years of diagnosis.
- Able to demonstrate the capacity to provide informed consent to take part in this feasibility trial, as assessed by their own clinician.
Exclusion Criteria:
- Active DSM-V substance abuse (except nicotine or caffeine) or dependence within the last three months
- Relevant CNS or other medical disorders
- Diagnosis of Learning Disability.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Experimental
No Intervention
Arm Label
Individual Placement and Support (IPS)
Cognitive Remediation Therapy (CRT)
IPS and CRT
Treatment as usual
Arm Description
IPS is a vocational support program to facilitate return to employment in individuals with severe and enduring mental illnesses.
CRT will be delivered twice weekly individual computerised CRT with therapist input. This therapy will be delivered by a CRT trained assistant psychologist.
A combination of IPS and CRT will be provided to participants in this arm.
Continued input as normal with treating psychiatrist.
Outcomes
Primary Outcome Measures
Feasibility of undertaking a trial of the intervention, as determined by: Recruitment and attrition rates
Recruitment and attrition rates: This will be determined using recruitment and attrition rates into the trial
Acceptability of the intervention, as determined by: number of sessions attended
Therapy logs: therapy logs with number of sessions attended
Client Satisfaction Questionnaire (CSQ)
Participants' satisfaction will be measured using CSQ-8. The scale consists of 8 items score range from 8 to 32, with higher values indicating higher satisfaction.
Secondary Outcome Measures
Full Information
NCT ID
NCT03974620
First Posted
May 18, 2019
Last Updated
August 25, 2023
Sponsor
Pakistan Institute of Living and Learning
1. Study Identification
Unique Protocol Identification Number
NCT03974620
Brief Title
Individual Placement and Support and/or Cognitive Remediation Therapy Added to TAU in Patients With Early Schizophrenia
Official Title
Individual Placement and Support (IPS) and Cognitive Remediation Therapy (CRT) as an Adjunct to Treatment as Usual (TAU) in Patients With Early Schizophrenia Spectrum Disorder: Study Protocol for a Randomized Controlled Feasibility Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
December 1, 2023 (Anticipated)
Primary Completion Date
December 30, 2024 (Anticipated)
Study Completion Date
December 30, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pakistan Institute of Living and Learning
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
This study aims to test the hypothesis that addition of Individual Placement and Support (IPS) and/or Cognitive Remediation Therapy (CRT) in addition to treatment as usual in patients with early psychosis will be feasible and acceptable in patients with early schizophrenia.
Detailed Description
This is an assessor blind, randomised controlled trial, employing a factorial design. This trial aims to assess the feasibility of IPS, CRT or their combination as an add on to treatment as usual. Patients with early schizophrenia spectrum disorder will be recruited from major psychiatric units in Pakistan. Treatment as usual (TAU) will comprise of patient's current antipsychotic medication as prescribed by their responsible clinician. Patients will be randomised into IPS, CRT, their combination or TAU, according to the 2x2 factorial schedule in the table. A total of 30 participants will be recruited in each cell, giving a total of 120 participants.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizophreniform Disorders, Schizoaffective Disorder, Psychosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Individual Placement and Support (IPS)
Arm Type
Experimental
Arm Description
IPS is a vocational support program to facilitate return to employment in individuals with severe and enduring mental illnesses.
Arm Title
Cognitive Remediation Therapy (CRT)
Arm Type
Experimental
Arm Description
CRT will be delivered twice weekly individual computerised CRT with therapist input. This therapy will be delivered by a CRT trained assistant psychologist.
Arm Title
IPS and CRT
Arm Type
Experimental
Arm Description
A combination of IPS and CRT will be provided to participants in this arm.
Arm Title
Treatment as usual
Arm Type
No Intervention
Arm Description
Continued input as normal with treating psychiatrist.
Intervention Type
Behavioral
Intervention Name(s)
Individual Placement and Support
Intervention Description
Individual Placement and Support is a vocational support program that was developed in the USA, to facilitate return to employment in individuals with severe and enduring mental illnesses.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Remediation Therapy
Intervention Description
This is an evidence based intervention that aims to improve cognitive functioning.
Primary Outcome Measure Information:
Title
Feasibility of undertaking a trial of the intervention, as determined by: Recruitment and attrition rates
Description
Recruitment and attrition rates: This will be determined using recruitment and attrition rates into the trial
Time Frame
6 month post intervention
Title
Acceptability of the intervention, as determined by: number of sessions attended
Description
Therapy logs: therapy logs with number of sessions attended
Time Frame
6 months post intervention
Title
Client Satisfaction Questionnaire (CSQ)
Description
Participants' satisfaction will be measured using CSQ-8. The scale consists of 8 items score range from 8 to 32, with higher values indicating higher satisfaction.
Time Frame
6 month post intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male/Female patients aged between 18-35 years.
Diagnosis of schizophrenia confirmed by SCID meeting DSM-V criteria for schizophrenia, schizophreniform or schizoaffective psychosis.
Stable on medication for the past four weeks.
In contact with mental health services
Within 5 years of diagnosis.
Able to demonstrate the capacity to provide informed consent to take part in this feasibility trial, as assessed by their own clinician.
Exclusion Criteria:
Active DSM-V substance abuse (except nicotine or caffeine) or dependence within the last three months
Relevant CNS or other medical disorders
Diagnosis of Learning Disability.
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Anonymised data once analysed and published will be available on reasonable request.
Learn more about this trial
Individual Placement and Support and/or Cognitive Remediation Therapy Added to TAU in Patients With Early Schizophrenia
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