A Study to Evaluate the Utilization and Benefits of Autonomous Sensory Meridian Response (ASMR) in Patients with Fibromyalgia

Overview

About this study

The primary purpose of this study is to assess the rate of utilization of Autonomous Sensory Meridian Response (ASMR) in our cohort of patients with fibromyalgia (FM).

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Patient age 18 or above.
Patients must understand and provide written informed consent and HIPAA authorization prior to initiation of any study-specific procedures.

Exclusion Criteria:

Schizophrenia.
Inability to provide informed consent.
Inability to speak/read English.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status	Contact
Rochester, Minn. Mayo Clinic principal investigator Arya Mohabbat, M.D.	Closed for enrollment	Contact information: Arya Mohabbat M.D. (507) 283-4849 Mohabbat.Arya@mayo.edu

Mayo Clinic Location

Status

Contact

Rochester, Minn.

Mayo Clinic principal investigator

Arya Mohabbat, M.D.

Closed for enrollment

Contact information:

Arya Mohabbat M.D.

(507) 283-4849

Mohabbat.Arya@mayo.edu

More information

Publications

Publications are currently not available

Clinical Trials