Integrated Behavioral Health Techniques in Patients with Fibromyalgia
Overview
Tab Title Description
Study type
ObservationalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Rochester, Minnesota: 24-007579
About this study
The purpose of this study is to assess the feasibility of implementing a virtual longitudinal behavioral health regimen (via Lin Health) in patients with fibromyalgia, seen at the Fibromyalgia and Chronic Fatigue Clinic at Mayo Clinic (Rochester), to assess the overall clinical impact of integrating virtual longitudinal behavioral health techniques in patients with fibromyalgia, to identify any demographic differences or clinical outcome differences in patients with fibromyalgia based on study enrollment payment type (private pay vs insurance), and to study the benefits and barriers of implementing a virtual longitudinal behavioral health regimen (via Lin Health) in patients with fibromyalgia, seen at Mayo Clinic
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 must be 18 years of age or older.
- Patient must have a diagnosis of Fibromyalgia.
- Patient must be being seen at the Mayo Clinic Fibromyalgia and Chronic Fatigue Clinic in Rochester, MN.
- Patient must be able to understand and provide informed consent and HIPAA authorization
- Patient must be willing and able to complete all aspects of the study.
- Patient must be able to speak and read English.
Exclusion Criteria:
- Patient who is under the age of 18 years old.
- Patient who is unable to provide informed consent or HIPAA authorization.
- Patient who declines study participation.
- Patient who is unable to speak English.
- Patient who is on active cancer therapy.
- Patient who is actively psychotic or actively suicidal.
- Patient who is deemed inappropriate to the study by the medical professional.
Note: Other protocol defined Inclusion/Exclusion Criteria may apply.
Eligibility last updated 07/26/2024. Questions regarding updates should be directed to the study team contact.
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 |
|
Rochester, Minn.
Mayo Clinic principal investigator Arya Mohabbat, M.D. |
Closed for enrollment |
|
More information
Publications
Publications are currently not available