Actively Recruiting
Virtual Patient Groups for Sarcoidosis Associated Fatigue
Led by The Cleveland Clinic · Updated on 2026-04-24
100
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
Sponsors
T
The Cleveland Clinic
Lead Sponsor
N
National Institute on Minority Health and Health Disparities (NIMHD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research study is testing whether Mindfulness-Based Stress Reduction (MBSR) can help reduce fatigue in people with sarcoidosis. The study will also look at whether MBSR can improve symptoms of anxiety and depression. Participants will be placed into one of two groups: * One group will take part in an 8-week virtual MBSR program, attend weekly online sessions, keep a daily mindfulness journal, and complete surveys about fatigue, anxiety, and depression. * The other group will join a virtual support group once a month for 5 months and complete the same surveys. The goal is to see which approach is more helpful for improving fatigue and mental well-being in people with sarcoidosis.
CONDITIONS
Official Title
Virtual Patient Groups for Sarcoidosis Associated Fatigue
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Self reported diagnosis of sarcoidosis
- Fatigue with Fatigue Assessment Scale (FAS) score of 22 or higher
- Age 18 years or older
- Ability to speak and read English
- Access to internet
- Capacity to consent
You will not qualify if you...
- Current daily meditation practice
- Previous participation in formal mindfulness-based interventions such as MBSR, MBCT, Acceptance and Commitment therapy, or Dialectical Behavior Therapy
- Any condition making the participant unsuitable for group intervention, including suicidal ideation
- No access to any form of online video
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cleveland Clinic
Cleveland, Ohio, United States, 44195
Actively Recruiting
Research Team
T
Tiana Powell
CONTACT
L
Logan J Harper, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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