Clinical trial · Interventional
An Exploratory Study to Evaluate Attention Biases in Adults With Multiple Sclerosis, Breast Cancer, and Lung Cancer
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
CT-100 is a platform that provides interactive, software based therapeutic components that may be used as part of a treatment in future software-based prescription digital therapeutics. One class of CT-100 components are Digital Neuro-activation and Modulation (DiNaMo) components. DiNaMo components target key neural systems (including but not limited to systems related to sensory-, perceptual-, affective-, pain-, attention-, cognitive control, social- and self-processing) to optimally improve a participant's health.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Lung Cancer | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
| Multiple Sclerosis | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CT-100-D-004-A | Device | — | UNRESOLVED |
| CT-100-D-004-B | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (8)
- type
- EXPERIMENTAL
- label
- Multiple Sclerosis with Mobility Limitations Study App A
- description
- Cognitive Training App CT-100-D-004-A uses implicit training with audiovisual stimuli to potentially redirect and modulate attention processes. This intervention is designed to help improve cognitive capabilities as well as redirect attentional biases to make participants less sensitive to distressing stimuli for multiple sclerosis with mobility limitations.
- interventionNames
- Device: CT-100-D-004-A
- type
- OTHER
- label
- Multiple Sclerosis with Mobility Limitations Study App B
- description
- Cognitive Training App CT-100-D-004-B uses implicit training with verbal processing exercises to potentially redirect and modulate attention processes. This intervention is designed to help improve cognitive capabilities as well as redirect attentional biases to make participants less sensitive to distressing stimuli for multiple sclerosis with mobility limitations.
- interventionNames
- Device: CT-100-D-004-B
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 22 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: * A participant will be eligible for entry into the study if all of the following criteria are met: 1. Fluent in written and spoken English, confirmed by ability to read, understand, and sign the informed consent form 2. Lives in the United States 3. Adult between 22 and 65 years old 4. Meets indication-specific including criteria, as reported by the study participant with adequate clinical documentation (to be provided to the study team upon request) 5. Has an active email address and is willing and able to receive and respond to email messages 6. Has access to an internet connection during the study duration 7. Has an active PayPal account to receive study compensation, or is willing to create one 8. Willing and able to comply with study protocol and assessments 9. Is the sole user of an iPhone with an iPhone operating system (iOS) version 14 or later or a smartphone with an Android operating system (OS) version 10 or later for the duration of the study 10. Is willing and able to receive Short Message Service (SMS) text messages and notifications on their smartphone 11. Has access to operating headphones Exclusion Criteria: * A participant will not be eligible for study entry if any of the following criteria are met: 1. Visual, dexterity or cognitive deficit so severe that it precludes the use of an App-based reaction time-based activity per investigator judgment 2. Severe psychiatric disorder involving a history of psychosis (e.g., schizophrenia, bipolar disorder, severe personality disorders) 3. Psychiatric hospitalization in the past 6 months 4. Participation in any research study (including studies on psychotherapy, mindfulness, cognitive training or pharmacological treatment) during the past 3 months 5. Initiation or change in primary disease-specific medication within 30 days prior to entering the study 6. Planning the introduction of new therapies (including studies on psychotherapy, mindfulness, cognitive training or pharmacological treatment) during the study duration (6 weeks) 7. Anticipating a change in current pharmacological or psychotherapy treatment regimen during the study period (6 weeks) 8. Self-reported substance use disorder within the past 1 year 9. Severe neurological disorders impairing brain function (e.g., previous stroke, dementia, primary brain function, brain metastases, Alzheimer's disease, Parkinson's disease, history of significant head trauma followed by persistent neurologic deficits or known structural brain abnormalities) 10. Mild, moderate, severe or profound unilateral or bilateral hearing loss
References
Publications (0)
Data not yet available