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CURATE.AI COR-Tx Trial for Post Brain Radiotherapy Patients

Primary Purpose

Cognitive Decline

Status
Recruiting
Phase
Not Applicable
Locations
Singapore
Study Type
Interventional
Intervention
CURATE.AI
Sponsored by
National University Hospital, Singapore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cognitive Decline focused on measuring Oncology, Digital therapeutics, Cognitive evaluation, Digital diagnostic, Cognitive training, Phenotypic Personalised Medicine (PPM), Multi-Attribute Task Battery (MATB), Training intensity, Radiotherapy, CURATE.AI

Eligibility Criteria

21 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age >21 years.
  • ECOG performance status 0 to 2.
  • Patients with a neoplastic condition (benign or malignant) involving the brain or skull requiring radiotherapy (with or without chemotherapy).
  • Patients with a life expectancy of at least 6 months.

Exclusion Criteria:

  • Pregnant or breastfeeding women.
  • Patients undergoing stereotactic radiosurgery (single fraction).
  • Patients who are undergoing re-irradiation to the same area of the brain.
  • Patients physically incapable of using computer tablet (either due to vision loss or dominant hand weakness)
  • Patients who cannot understand spoken English language.
  • Patients who are unable to give informed consent.

Sites / Locations

  • National University HospitalRecruiting
  • The N.1 Institute for Health (N.1), NUSRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

CURATE.AI

Arm Description

A cognitive evaluation and a Digital Diagnostic (DD) session performed anytime before radiotherapy will serve as the baseline. After the radiotherapy treatment, which can last between 1 to 6.5 weeks, patients will have a variable recovery time (0 to 4 weeks). Subsequently, patients will be subject to a cognitive evaluation and a DD session, right before starting the Digital Intervention (DI) training. This training will comprise ten weeks of DI (three 10-15 minute sessions per week). Patients will complete cognitive evaluations and DD sessions at the end of DI, and 16 and 32 weeks after the end of DI.

Outcomes

Primary Outcome Measures

Patient acceptability of the digital cognitive test battery DI/DD obtained during a semi-structured interview
Qualitative summary of patient acceptability of the digital cognitive test battery DI/DD
Patient adherence to the DI/DD
Percentage of completed DI/DD sessions
Patient attrition rate to the DI/DD
Percentage of patients that drop out of DI/DD
Percentage of CURATE.AI profiles successfully created and applied
Timely delivery of DI/DD at indicated time points
Percentage of DI/DD sessions successfully delivered by study team at indicated time points
Digital intervention limited efficacy
Change in cognitive performance as measured by the standard of care cognitive evaluations pre-post digital intervention
Digital diagnostic limited efficacy
Correlation between standard of care cognitive evaluations scores and digital diagnostic scores

Secondary Outcome Measures

1. Usability of the digital cognitive test battery DI/DD obtained during a semi-structured interview
Qualitative summary of patient usability of the digital cognitive test battery DI/DD

Full Information

First Posted
March 2, 2021
Last Updated
November 10, 2021
Sponsor
National University Hospital, Singapore
Collaborators
National University of Singapore, The N.1 Institute for Health (N.1)
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1. Study Identification

Unique Protocol Identification Number
NCT04848935
Brief Title
CURATE.AI COR-Tx Trial for Post Brain Radiotherapy Patients
Official Title
CURATE.AI Optimised Digital COgnitive Rehabilitation Therapy (COR-Tx) for Post Brain Radiotherapy Patients: CURATE.AI COR-Tx Mixed-methods Feasibility Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Recruiting
Study Start Date
June 14, 2021 (Actual)
Primary Completion Date
January 1, 2022 (Anticipated)
Study Completion Date
July 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National University Hospital, Singapore
Collaborators
National University of Singapore, The N.1 Institute for Health (N.1)

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
Cognitive deficit is common in patients who have undergone whole brain or partial brain radiotherapy. To counteract intellectual deterioration, the conventional strategies includes drug- based treatments such as donezepil and memantine, which have shown to only provide marginal improvement and, cognitive training regimens, both of which are usually administered at fixed dose/intensities often leading to sub-optimal responses. This study aims to address this clinically relevant problem by harnessing the CURATE.AI platform to identify N-of-1cognitive training profiles the can enhance learning trajectories through individualised calibration and training regimens. CURATE.AI is a phenotypic personalised medicine (PPM) platform that correlates a patient's phenotypic response (cognitive performance) to a certain input (training intensity) based exclusively on the patient's data. This PPM platform is independent of biological system or interventional agent and can be applied to any disorder treatment where dosing/intensity could be better personalised. CURATE.AI is expected to optimise/personalise cognitive training in post-brain radiotherapy patients by dynamically modulating the intensity of a digital cognitive test battery that measures executive processing, multitasking and perceptual learning tasks. In addition, this clinical feasibility trial aims to assess this cognitive test battery as a potential analogous or complementary diagnostic tool as compared to traditional cognitive evaluations performed by a clinician.
Detailed Description
Brain radiotherapy causes downstream cognitive deficits. Drug-based cognitive decline treatments show little improvement and side effects may reduce patient compliance. Regimens are usually administered at a fixed dose that doesn't incorporate high patient variability, leading to sub-optimal responses. Effective cognitive training can improve cognitive performance. Artificial intelligence platforms show great potential for training personalisation. The CURATE.AI platform can be used to identify N-of-1 (single subject) training profiles that can be used to optimise learning trajectories through individualised calibration and training regimens, potentially leading to improved outcomes compared to standard static or adaptive training strategies. CURATE.AI uses only a subject's own performance data to identify the intensity needed for his/her best output. As the subject evolves during the course of intervention, the training intensities are dynamically modulated to maintain performance within a given range. Here the investigators propose to test the feasibility of CURATE.AI, with a digital cognitive test battery as the interface, as an adaptive training platform for cognitive training addressed to improve brain cancer radiotherapy patients' cognitive performance. The acceptability, implementation and limited efficacy of the digital intervention (DI) will be explored. In addition, the investigators propose to test the feasibility of the digital cognitive test battery potential as a digital diagnostic (DD) tool as compared to traditional cognitive evaluations performed by a clinician. User experience and usability will also be explored.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cognitive Decline
Keywords
Oncology, Digital therapeutics, Cognitive evaluation, Digital diagnostic, Cognitive training, Phenotypic Personalised Medicine (PPM), Multi-Attribute Task Battery (MATB), Training intensity, Radiotherapy, CURATE.AI

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CURATE.AI
Arm Type
Experimental
Arm Description
A cognitive evaluation and a Digital Diagnostic (DD) session performed anytime before radiotherapy will serve as the baseline. After the radiotherapy treatment, which can last between 1 to 6.5 weeks, patients will have a variable recovery time (0 to 4 weeks). Subsequently, patients will be subject to a cognitive evaluation and a DD session, right before starting the Digital Intervention (DI) training. This training will comprise ten weeks of DI (three 10-15 minute sessions per week). Patients will complete cognitive evaluations and DD sessions at the end of DI, and 16 and 32 weeks after the end of DI.
Intervention Type
Device
Intervention Name(s)
CURATE.AI
Intervention Description
CURATE.AI will be utilised to provide personalised training intensity recommendations (low, medium or high) to the patients during the digital cognitive test battery DI session. The difficulty of each task will be modulated by CURATE.AI by adjusting the frequency of critical events that demand evaluation and/or response.
Primary Outcome Measure Information:
Title
Patient acceptability of the digital cognitive test battery DI/DD obtained during a semi-structured interview
Description
Qualitative summary of patient acceptability of the digital cognitive test battery DI/DD
Time Frame
One visit 60 minutes (at the end of the 10 week intervention)
Title
Patient adherence to the DI/DD
Description
Percentage of completed DI/DD sessions
Time Frame
up to 12 months
Title
Patient attrition rate to the DI/DD
Description
Percentage of patients that drop out of DI/DD
Time Frame
up to 12 months
Title
Percentage of CURATE.AI profiles successfully created and applied
Time Frame
up to 12 months
Title
Timely delivery of DI/DD at indicated time points
Description
Percentage of DI/DD sessions successfully delivered by study team at indicated time points
Time Frame
up to 12 months
Title
Digital intervention limited efficacy
Description
Change in cognitive performance as measured by the standard of care cognitive evaluations pre-post digital intervention
Time Frame
up to 12 months
Title
Digital diagnostic limited efficacy
Description
Correlation between standard of care cognitive evaluations scores and digital diagnostic scores
Time Frame
up to 12 months
Secondary Outcome Measure Information:
Title
1. Usability of the digital cognitive test battery DI/DD obtained during a semi-structured interview
Description
Qualitative summary of patient usability of the digital cognitive test battery DI/DD
Time Frame
One visit 60 minutes (at the end of the 10 week intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >21 years. ECOG performance status 0 to 2. Patients with a neoplastic condition (benign or malignant) involving the brain or skull requiring radiotherapy (with or without chemotherapy). Patients with a life expectancy of at least 6 months. Exclusion Criteria: Pregnant or breastfeeding women. Patients undergoing stereotactic radiosurgery (single fraction). Patients who are undergoing re-irradiation to the same area of the brain. Patients physically incapable of using computer tablet (either due to vision loss or dominant hand weakness) Patients who cannot understand spoken English language. Patients who are unable to give informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dr Balamurugan A Vellayappan
Phone
+65 67795555
Email
bala_vellayappan@nuhs.edu.sg
First Name & Middle Initial & Last Name or Official Title & Degree
Qian Yee, Queenie Chai
Email
queenie_qy_chai@nuhs.edu.sg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr Balamurugan A Vellayappan
Organizational Affiliation
National University Cancer Institute, Singapore
Official's Role
Principal Investigator
Facility Information:
Facility Name
National University Hospital
City
Singapore
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Qian Yee, Queenie Chai, Coordinator
Email
queenie_qy_chai@nuhs.edu.sg
First Name & Middle Initial & Last Name & Degree
Fatin Aliyah, Coordinator
Email
fatin_hussin@nuhs.edu.sg
Facility Name
The N.1 Institute for Health (N.1), NUS
City
Singapore
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xavier Tadeo, PhD
Email
biextc@nus.edu.sg
First Name & Middle Initial & Last Name & Degree
Yoong Hun Ong, MSc
Phone
+6596680807
Email
yh.ong@nus.edu.sg
First Name & Middle Initial & Last Name & Degree
Agata Blasiak, PhD
First Name & Middle Initial & Last Name & Degree
Dean Ho, Prof
First Name & Middle Initial & Last Name & Degree
Theodore Kee, MSc
First Name & Middle Initial & Last Name & Degree
Alexandria Remus, PhD
First Name & Middle Initial & Last Name & Degree
Chris Asplund, A/Prof

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
Citation
Kee, Theodore & Weiyan, Chee & Blasiak, Agata & Chong, Jordan & Chen, Jonna & Yeo, B.T. Thomas & Ho, Dean & Asplund, Christopher. (2019). Harnessing CURATE.AI as a Digital Therapeutics Platform by Identifying N-of-1 Learning Trajectory Profiles. Advanced Therapeutics. 2. 1900023. 10.1002/adtp.201900023.
Results Reference
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PubMed Identifier
27053773
Citation
Zarrinpar A, Lee DK, Silva A, Datta N, Kee T, Eriksen C, Weigle K, Agopian V, Kaldas F, Farmer D, Wang SE, Busuttil R, Ho CM, Ho D. Individualizing liver transplant immunosuppression using a phenotypic personalized medicine platform. Sci Transl Med. 2016 Apr 6;8(333):333ra49. doi: 10.1126/scitranslmed.aac5954.
Results Reference
background
Citation
Pantuck AJ, Lee DK, Kee T, Wang P, Lakhotia S, Silverman MH, Mathis C, Drakaki A, Belldegrun AS, Ho CM, Ho D. Modulating BET bromodomain inhibitor ZEN-3694 and enzalutamide combination dosing in a metastatic prostate cancer patient using CURATE. AI, an artificial intelligence platform. Advanced Therapeutics. 2018 Oct;1(6):1800104.
Results Reference
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CURATE.AI COR-Tx Trial for Post Brain Radiotherapy Patients

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