Study of Two Digital Therapeutics for the Prevention of Episodic Migraine

NCT ID: NCT05853900

Last Updated: 2025-07-03

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 568 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-03-28
• Study Completion Date: 2024-05-07

Brief Summary

Randomized study of two digital therapeutics for the prevention of episodic migraine

Detailed Description

The purpose of this randomized ReMMi-D trial is to evaluate the effectiveness and safety of two prescription mobile applications that provide an interactive, software-based intervention for the preventative treatment of episodic migraine in late adolescents and adults.

Conditions

Migraine; Episodic Migraine; Headache; Headache, Migraine

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Arm A

Mobile application A as a software-based intervention for the preventive treatment of episodic migraine in late adolescents and adults.

Group Type: EXPERIMENTAL

ReMMi-D Digital Therapeutic

Intervention Type: DEVICE

Evaluate the effectiveness and safety of prescription mobile applications that provide an interactive, software-based intervention for the preventative treatment of episodic migraine in late adults and adolescents.

Arm B

Mobile application B is an investigational digital therapeutic that is being studied for the preventative treatment of episodic migraine.

Group Type: EXPERIMENTAL

ReMMi-D Digital Therapeutic

Intervention Type: DEVICE

Evaluate the effectiveness and safety of prescription mobile applications that provide an interactive, software-based intervention for the preventative treatment of episodic migraine in late adults and adolescents.

Interventions

ReMMi-D Digital Therapeutic

Evaluate the effectiveness and safety of prescription mobile applications that provide an interactive, software-based intervention for the preventative treatment of episodic migraine in late adults and adolescents.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• A participant will be eligible for entry into the study if all of the following criteria are met:

1. Willing and able to provide written informed consent to participate in the study, attend study visits, and comply with study-related requirements and assessments.

2. Lives in the United States.

3. Adult or late adolescent, 18 years of age or older at the time of informed consent.

4. Fluent in written and spoken English, confirmed by ability to read and understand the informed consent form.

5. The following will be physician-reviewed: Participant has at least a 1-year history of migraine (with or without aura) consistent with a diagnosis according to the International Classification of Headache Disorders, 3rd Edition.

1. Age of onset of migraines prior to 50 years of age

2. Migraine attacks, on average, lasting 4-72 hours if untreated

3. Per participant report, 4-14 migraine days per month within the last 3 months prior to the Screening Visit (a month is defined as 28 days)

4. Four to fourteen migraine days during the run-in period

6. Is currently managing migraines with ≥1 prescription acute treatment and/or prescription first or second-line preventive medications, as assessed by a physician.

7. Is the sole user of an iPhone with an iPhone operating system (iOS) 14 or later or a smartphone with an Android operating system (OS) 11 or later and is willing to download and use the Study App required by the protocol.

8. Is willing and able to receive SMS text messages and push messages on their smartphone.

9. Is the owner of, and has regular access to, an email address.

10. Has regular access to the Internet via cellular data plan and/or wifi.

Exclusion Criteria

• A participant will not be eligible for study entry if any of the following criteria are met:

1. History of basilar migraine or hemiplegic migraine.

2. Active chronic pain syndromes, such as fibromyalgia, chronic pelvic pain, or complex regional pain syndrome (CRPS).

3. Other pain syndromes (including trigeminal neuralgia), psychiatric conditions (such as major depressive episode, bipolar disorder, major depressive disorder, schizophrenia), dementia, or significant neurological disorders (other than migraine) that, in the Investigator's opinion, might interfere with study assessments.

4. History of, treatment for, or evidence of, alcohol or drug abuse within the past 12 months (48 weeks) or having met DSM-V criteria for any significant substance use disorder within the past 12 months (48 weeks) from the date of the screening visit.

5. History of use of analgesics (e.g., nonsteroidal anti-inflammatory drugs [NSAIDs] or acetaminophen, including opioids) or butalbital on ≥ 15 days per month during the 3 months (12 weeks) prior to the Screening Visit or during the run-in period.

6. Currently taking a prescription anti-calcitonin gene-related peptide (CGRP) for either episodic or chronic migraine.

7. Post-traumatic headache, persistent post-traumatic headache, or post-concussion syndrome.

8. Other significant episodic or chronic medical condition(s) that in the opinion of the Investigator, may confound the interpretation of findings to inform PDT development.

9. Failure to adhere with or inability to complete Study App inputs and onboarding activities during the run-in period. Participants who are not adherent during the run-in period are not eligible for study entry.

10. Previous enrollment in any digital therapeutics pilot or pivotal study for a migraine indication.

11. Participation in any other investigational clinical study while participating in this clinical study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Click Therapeutics, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Parth Shah

Role: PRINCIPAL_INVESTIGATOR

ObvioHealth

Locations

Click Therapeutics

New York, New York, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

CT-132-R-001

Identifier Type: -

Identifier Source: org_study_id