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Cognitive Behavior Therapy (CBT) Informed Mobile-Application for First Episode Psychosis (TechCare)

Primary Purpose

Psychosis

Status
Recruiting
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Cognitive Behavioral Therapy,
Sponsored by
Pakistan Institute of Living and Learning
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Psychosis focused on measuring Psychosis, mHealth, Techonology, LMICs

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • The inclusion criteria for the study will be:
  • Male and Females patients diagnosed with FEP- Schizophrenia or Schizoaffective disorder.
  • Over the age of 18 years.
  • A score of three or more on any of the positive symptoms on the PANSS
  • A Minimum score of one on the Calgary Depression scale (CDS)
  • Having smart phone and able to use smart phone functions.
  • Able to understand written and spoken Urdu.

Exclusion Criteria:

  • Exclusions will be any evidence of organic brain disease, clinically significant concurrent medical illness, learning disability.
  • unable to use simple functions of an android phone

Sites / Locations

  • Institute of PsychiatryRecruiting
  • Civil HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

TechCare

Wait-List control group:

Arm Description

Participants in this arm will receive a mobile app based cognitive behavior therapy informed "TechCare" intervention for a period of 12 weeks.

Participants in this arm will be offered the intervention once the intervention arm have completed their 3rd month outcome assessment.

Outcomes

Primary Outcome Measures

Feasibility measures
Feasibility will be determined by recruitment rates, adherence rate and retention rates. The criterion for success of feasibility is to recruit >50% of eligible participants, adherence rate (number of home assignments completed; > 50%) and retention rate of 70%
Acceptability measure
Acceptability will be determined using participant feedback on the use of app

Secondary Outcome Measures

Positive and Negative Syndrome Scale
The Scale will indicate the Positive and Negative Syndrome for Schizophrenia that has been comprised of 30 items. The 30 items of semi structured questionnaire will measure positive syndromes, like delusions, hallucinations and conceptual disorganization whereas negative syndromes include passive or apathetic social avoidance and blunted affect.
Psychotic Symptom Rating Scales (PSYRATS)
The dimensions of hallucinations and delusions will be measured by a semi structured interview scale . The dimensions of hallucinations and delusions will be measured by a semi structured interview scale
Calgary Depression Scale (CDS)
The scale is specially designed to measure the depression for Psychosis, consist of nine items (Addington et al., 1990). CDS will indicate the subjective and qualitative dimensions of depression in Schizophrenia.
The Work and Social Adjustment Scale (WSAS)
Five items scale that measures the perceived impairment of social life, relationships, home management, work and private leisure having scores between 0 to 8 that means 0 (no impairment) and 8 (very severe impairment) with a total score of 40 (Mundt, Marks, Shear, & Greist, 2002).
EuroQol-5 Dimensions EQ5-D
An instrument measures the health-related quality of life. Quality of life will be measured in five dimensions, including usual activities, anxiety/depression, pain/discomfort, self-care and mobility (Sobocki et al 2007).
Client Service Receipt Inventory (CSRI):
We will collect information about the use of other health services (including the informal sector faith healers/Imams) using CSRI.

Full Information

First Posted
October 1, 2022
Last Updated
October 1, 2022
Sponsor
Pakistan Institute of Living and Learning
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1. Study Identification

Unique Protocol Identification Number
NCT05567575
Brief Title
Cognitive Behavior Therapy (CBT) Informed Mobile-Application for First Episode Psychosis
Acronym
TechCare
Official Title
Culturally Adapted Cognitive Behavior Therapy (CBT) Informed Mobile-Application for First Episode Psychosis (FEP). A Feasibility Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2022 (Actual)
Primary Completion Date
December 30, 2024 (Anticipated)
Study Completion Date
July 31, 2025 (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
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Onset of First Episode Psychosis (FEP) is at a young age and is a critical period influencing the long-term course of the disorder. Failure to identify FEP can lead to serious implications such as disruption of education, reduced long-term employment, huge economic burden, and is associated with significantly higher mortality. The prevalence of psychosis increases rapidly from age 14 onwards with a peak incidence in the late teens and early 20s. The aim of the project is to examine the acceptability and feasibility of a mobile phone application-based intervention 'TechCare-PK', for individuals with psychosis in Pakistan. The main objectives are to determine whether appropriate individuals could be identified and recruited to the study and whether the TechCare App would be an acceptable intervention for individuals with psychosis.
Detailed Description
Onset of First Episode Psychosis (FEP) is at a young age and is a critical period influencing the long-term course of the disorder. Failure to identify FEP can lead to serious implications such as disruption of education, reduced long-term employment, huge economic burden, and is associated with significantly higher mortality. The prevalence of psychosis increases rapidly from age 14 onwards with a peak incidence in the late teens and early 20s. The aim of the project is to examine the acceptability and feasibility of a mobile phone application-based intervention 'TechCare-PK', for individuals with psychosis in Pakistan. The main objectives are to determine whether appropriate individuals could be identified and recruited to the study and whether the TechCare App would be an acceptable intervention for individuals with psychosis. Where there are challenges related to distance, inconvenience, being homebound or reluctance to face-to-face interventions, Mobile Health (mHealth) approaches that leverage mobile devices such as cellular phones and smartphones can be used to support healthcare system. Research has found mobile based interventions as highly acceptable to families and may meet carers' needs in respect of information, guidance, professional and emotional support. These services has been considered as a good and easy mode of exchanging information, providing health related education and advice, management of symptoms, to early recognize the complications, giving reassurance and for providing quality services. Methods: Study Design: A multi-center single blind Randomised Controlled Trial (RCT) comparing with Treatment as Usual (TAU) with participants with First Episode Psychosis (FEP) to be recruited from different psychiatric units across four cities in Pakistan i.e., Karachi, Lahore, Hyderabad and Rawalpindi, Pakistan. If required additional centers will be added i.e., Quetta, Multan and Peshawar following proper ethics amendments. Aim The aim of this study is to design, and test culturally adapted mobile based CBT intervention for patients with FEP. Objectives: Develop and refine an app based intervention (TechCare) based on existing culturally adapted intervention for psychosis, using patient and public involvement. The aim is to improve its potential efficacy, establish acceptability of the refined intervention to potential participants and facilitators and establish mobile app based deliverability of the intervention To explore the usefulness of TechCare as an acceptable intervention in reducing symptoms of psychosis. Undertake an internal pilot to establish recruitment and attrition rates, compliance with protocol and acceptability of the trial design to participants. The proposed study will consist of three phases. First phase of study will focus on developing the app based intervention (TechCare) through qualitative work. Second phase will test run the application with 6-8 service users and incorporate suggestions and refinement of intervention and in the third phase we will test it in a randomised controlled trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psychosis
Keywords
Psychosis, mHealth, Techonology, LMICs

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Outcomes Assessor
Masking Description
Researchers doing outcome assessments will be kept masked of the treatment allocation
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TechCare
Arm Type
Experimental
Arm Description
Participants in this arm will receive a mobile app based cognitive behavior therapy informed "TechCare" intervention for a period of 12 weeks.
Arm Title
Wait-List control group:
Arm Type
Active Comparator
Arm Description
Participants in this arm will be offered the intervention once the intervention arm have completed their 3rd month outcome assessment.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Behavioral Therapy,
Other Intervention Name(s)
Mobile Health
Intervention Description
TechCare is based on the intelligent real time therapy (iRTT) conceptual model proposed by Kelly et al. iRTT relates to the use of mobile technologies to deliver interventions such as CBT, extending beyond assessment of symptoms. The intervention is based on the treatment manual developed by David G. Kingdon and Douglas Turkington. The intervention is informed by evidence based cognitive models of psychosis, where the participant is able to choose from a list of pre-selected digital self-help strategies that are personalised to each participant. For example, the App may incorporate the participant's favourite music in the form of multimedia or YouTube links, which are prompted during symptom elevation. Other examples may include psychoeducation, goal setting, problem-solving, etc., based on common self-help strategies in CBT for Psychosis (CBTp).
Primary Outcome Measure Information:
Title
Feasibility measures
Description
Feasibility will be determined by recruitment rates, adherence rate and retention rates. The criterion for success of feasibility is to recruit >50% of eligible participants, adherence rate (number of home assignments completed; > 50%) and retention rate of 70%
Time Frame
From baseline to 3rd month (at the end of intervention)
Title
Acceptability measure
Description
Acceptability will be determined using participant feedback on the use of app
Time Frame
From baseline to 3rd month (at the end of intervention)
Secondary Outcome Measure Information:
Title
Positive and Negative Syndrome Scale
Description
The Scale will indicate the Positive and Negative Syndrome for Schizophrenia that has been comprised of 30 items. The 30 items of semi structured questionnaire will measure positive syndromes, like delusions, hallucinations and conceptual disorganization whereas negative syndromes include passive or apathetic social avoidance and blunted affect.
Time Frame
Changes from baseline to week-12
Title
Psychotic Symptom Rating Scales (PSYRATS)
Description
The dimensions of hallucinations and delusions will be measured by a semi structured interview scale . The dimensions of hallucinations and delusions will be measured by a semi structured interview scale
Time Frame
Changes from baseline to week-12
Title
Calgary Depression Scale (CDS)
Description
The scale is specially designed to measure the depression for Psychosis, consist of nine items (Addington et al., 1990). CDS will indicate the subjective and qualitative dimensions of depression in Schizophrenia.
Time Frame
Changes from baseline to week-12
Title
The Work and Social Adjustment Scale (WSAS)
Description
Five items scale that measures the perceived impairment of social life, relationships, home management, work and private leisure having scores between 0 to 8 that means 0 (no impairment) and 8 (very severe impairment) with a total score of 40 (Mundt, Marks, Shear, & Greist, 2002).
Time Frame
Changes from baseline to week-12
Title
EuroQol-5 Dimensions EQ5-D
Description
An instrument measures the health-related quality of life. Quality of life will be measured in five dimensions, including usual activities, anxiety/depression, pain/discomfort, self-care and mobility (Sobocki et al 2007).
Time Frame
Changes from baseline to week-12
Title
Client Service Receipt Inventory (CSRI):
Description
We will collect information about the use of other health services (including the informal sector faith healers/Imams) using CSRI.
Time Frame
Changes from baseline to week-12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: The inclusion criteria for the study will be: Male and Females patients diagnosed with FEP- Schizophrenia or Schizoaffective disorder. Over the age of 18 years. A score of three or more on any of the positive symptoms on the PANSS A Minimum score of one on the Calgary Depression scale (CDS) Having smart phone and able to use smart phone functions. Able to understand written and spoken Urdu. Exclusion Criteria: Exclusions will be any evidence of organic brain disease, clinically significant concurrent medical illness, learning disability. unable to use simple functions of an android phone
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ameer B Khoso, Mphil
Phone
02135871845
Email
ameer.bukhsh@pill.org.pk
First Name & Middle Initial & Last Name or Official Title & Degree
Zaib un Nisa, Mphil
Phone
02135871845
Email
zaibunnisa@pill.org.pk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Omair Husain, MD
Organizational Affiliation
Centre for Addiciton and Mental Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Psychiatry
City
Rawalpindi
State/Province
Punjab
Country
Pakistan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Asad Tamizuddin, MD
Facility Name
Civil Hospital
City
Karachi
State/Province
Sindh
ZIP/Postal Code
75500
Country
Pakistan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Haider Naqvi, FCPS
Phone
(021) 99215740

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Cognitive Behavior Therapy (CBT) Informed Mobile-Application for First Episode Psychosis

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