Adults 18 to 65, any sex, with Migraine. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Feasibility of TeleBMMPrimary· Week 0 through Week 12
Feasibility of the study will be based on patient adherence to the protocol. The number of treatment components participants complete (out of 20) will be tabulated. It is hypothesized that at least half of the participants will attend all four study sessions and complete all three self-guided modules. Dropouts will be included in the analysis. Results will be summarized using basic descriptive statistics.
Group
Value
95% CI
Telehealth Behavioral Migraine Management
14.2
± 5.6
Change in Quality of Life (Migraine Specific)Secondary· Change from Pre-treatment (Week 0) to Post-treatment (Week 12)
Change in Migraine-related disability over the prior 4 week period was assessed based on Version 2.1 of the Migraine Specific Quality of Life Questionnaire (MSQ). The MSQ is a 14-item survey assessing quality of life in people with migraine. Responses from the 14 Items (which are reverse-coded) encompassing three domains (Role Restriction - 7 items; Role Prevention - 4 items; and Emotional Function - 3 items) were rated on a 6-point scale ranging from 1 ("None of the time") to 6 ("All of the time"). Raw scores were summed and linearly converted to a 0-100 scale wherein higher scores are associ
Group
Value
95% CI
Telehealth Behavioral Migraine Management
9.3
± 27.6
Education Modules
-11.4
± 14.4
Change in Headache FrequencySecondary· Change from Week 0 to Week 12
Participants were asked to complete a daily headache diary, on which each 7 day week they denoted whether they have had a headache attack. Slope change from Week 0 to Week 12 is reported as a proportion of headache days/month (ranging from 0-1) and is summarized by study arm.
Group
Value
95% CI
Telehealth Behavioral Migraine Management
.13
± .004
Education Control
.18
± .017
Sponsor's own description
This project aims to develop the protocol and obtain feasibility and acceptability information for Telehealth Behavioral Migraine Management in a single-arm pre-post pilot study. The investigator and study team aim to recruit 20 people with migraine from the Montefiore Headache Center in the Bronx New York. Participants will receive the 12-week protocol including a mobile app headache diary, an online patient manual with interactive vignettes, 4 50-minute telehealth sessions, and 3 15-minute check-ins.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
NCT07419607 — MIGRAFIT: Evaluating a Group Therapy Program Combining Physical Activity, Progressive Muscle Relaxation and Psychoeducat
· NA
· recruiting
NCT07487701 — Migraine Prevention With the Remote Electrical Neuromodulation (REN) Wearable: A Real-world Evidence Study
· NA
· active not recruiting
NCT07343427 — Impact of GON PRF on Central Sensitization in Migraine Patients
· NA
· active not recruiting
NCT07336056 — Nerivio Efficacy Under High-Frequency Use
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· active not recruiting
NCT07385755 — Desvenlafaxine for Preventive Treatment of Frequent Migraines
· NA
· active not recruiting
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
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Sponsor: as reported to ClinicalTrials.gov by Albert Einstein College of Medicine
Last refreshed: 11 March 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03982316.