Improving Health Outcomes of Migraine Patients Who Present to the Emergency Department

Sponsor
NYU Langone Health (Other)
Overall Status
Withdrawn
CT.gov ID
NCT02945839
Collaborator
(none)
0
1
2
35.1
0

Study Details

Study Description

Brief Summary

Collectively, evidence shows that a combination of medication and behavioral therapy is most effective for migraine care. The ED is a critical point of contact with the health care system for many migraine patients; in current practice, it is a missed opportunity to initiate and establish a comprehensive migraine management paradigm. Behavioral headache treatments (e.g., progressive muscle relaxation (PMR), biofeedback, cognitive-behavioral therapy (CBT)) are effective migraine treatment options that are essentially free of side effects. PMR has also been successful as a technique that patients can do independently. Studies have shown that combination pharmacological-behavioral therapy is most effective for migraine treatment.

Several aspects of this study are innovative, including: 1. Initiation of preventive medication in a timely manner for migraineurs who present to the ED. 2. Introduction of PM+PMR in the ED at a time that can serve as a teachable moment. 3. Introduction of a smartphone application-based product (a minimal contact based behavioral therapy) in the ED setting to reduce headache disability, frequency, and intensity.

Condition or Disease Intervention/Treatment Phase
  • Drug: Preventative Medication (PM)
  • Behavioral: Enhanced Usual Care
  • Behavioral: PMR (progressive muscle relaxation therapy)
Phase 4

Detailed Description

Investigators will conduct a randomized trial to evaluate the impact of a comprehensive migraine treatment program on the quality of life for migraineurs with frequent and disabling headaches who present to the ED. The intervention (PM+PMR) will combine acute treatment, migraine preventive medication-topiramate, and the APP with PMR. Data from patients in the intervention group will be compared with data from an enhanced usual care (EUC) group to examine the efficacy of the combined treatment effects.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Improving Health Outcomes of Migraine Patients Who Present to the Emergency Department
Actual Study Start Date :
Dec 28, 2016
Anticipated Primary Completion Date :
Dec 1, 2019
Anticipated Study Completion Date :
Dec 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Acute Treatment+ED-initiated preventive medication +PMR

All subjects will be discharged on acute migraine therapy (naproxen, triptan) unless there is a contraindication and will also be started on topiramate (25mg/night) with a plan to increase the dose every week by 25 mg up to 100 mg/night. Subjects will receive medicine along with progressive muscle relaxation therapy

Drug: Preventative Medication (PM)
Subjects in the PM group will be given acute migraine medication, preventive medication (topiramate), and the APP with the PMR component. The smartphone app and/or the electronic pill bottles will be used to monitor adherence.
Other Names:
  • Topiramate
  • Behavioral: Enhanced Usual Care
    General Education Class consisting of basic migraine information of basic migraine information such as evidence-based ways to treat migraines: treat early, limit acute medications < 2-3 days/week, and call the primary care physician (PCP) if abortive medications are used more frequently.

    Behavioral: PMR (progressive muscle relaxation therapy)
    Technique for learning to monitor and control the state of muscular tension

    Active Comparator: Enhanced Usual Care (EUC)

    Subjects will be given a general education session consisting of basic migraine information such as evidence-based ways to treat migraines: treat early, limit acute medications < 2-3 days/week, and call the primary care physician (PCP) if abortive medications are used more frequently. Any migraine treatment decisions on discharge will be left up to the ED attending. The RC will load the APP onto the subjects' smart phones but the PMR component will be blocked on the version of the APP that they receive. All subjects will be asked to track headache frequency, intensity, and acute medication use on the APP.

    Behavioral: Enhanced Usual Care
    General Education Class consisting of basic migraine information of basic migraine information such as evidence-based ways to treat migraines: treat early, limit acute medications < 2-3 days/week, and call the primary care physician (PCP) if abortive medications are used more frequently.

    Outcome Measures

    Primary Outcome Measures

    1. Migraine Disability Assessment Scale (MIDAS) at 3 Months and Baseline [12 Weeks]

      A decrease of 3 points in the MIDAS score corresponds to a one day reduction in headache related disability per month, a clinically meaningful difference.

    Secondary Outcome Measures

    1. Perceived Stress Scale (PSS) [12 Weeks]

      PSS scores are obtained by reversing responses (e.g., 0 = 4, 1 = 3, 2 = 2, 3 = 1 & 4 = 0) to the four positively stated items (items 4, 5, 7, & 8) and then summing across all scale items. A short 4 item scale can be made from questions 2, 4, 5 and 10 of the PSS 10 item scale.

    2. Number of days/week treated with acute medications [12 Weeks]

    3. Number of drug administrations/week for acute medications [12 Weeks]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 64 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Meets migraine criteria based on Information in Study Manual or based on Headache expert opinion -4+ migraines a month

    • Migraine Disability Assessment (MIDAS) score >5.

    Exclusion Criteria:
    • Patients who have had Cognitive Behavioral Therapy, Biofeedback or other Relaxation Therapy in the past year;

    • Cognitive deficit or other physical problem with the potential to interfere with behavioral therapy; Alcohol or other substance abuse as determined by self-report or prior documentation in the medical record;

    • Opioid or barbiturate use 10+ days a month;

    • PHQ9 score of severe depression;

    • Unable or unwilling to follow a treatment program that relies on written and audio recorded materials;

    • Not having a smartphone.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 New York University School of Medicine New York New York United States 10016

    Sponsors and Collaborators

    • NYU Langone Health

    Investigators

    • Principal Investigator: Mia Minen, MD, New York University Medical School

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    NYU Langone Health
    ClinicalTrials.gov Identifier:
    NCT02945839
    Other Study ID Numbers:
    • 16-00548
    First Posted:
    Oct 26, 2016
    Last Update Posted:
    Nov 29, 2019
    Last Verified:
    Nov 1, 2019
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by NYU Langone Health
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 29, 2019