Cystic Fibrosis Wellness Program for Fatigue and Sleep Issues
CF Wellness Program
Recruiting
N/A
Interventional Study
Cystic Fibrosis (CF)
Fatigue
Sleep Quality
Insomnia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 80 (estimated)
- Sponsor
- Johns Hopkins University · Other
Who this trial is looking for
This trial is looking for adults with cystic fibrosis who are dealing with fatigue and sleep problems. Participants will join a wellness program and track their progress over time compared to usual care.
Are You a Good Fit for This Trial?
You may be able to join if
- I am 18 years old or older.
- I have a diagnosis of cystic fibrosis.
- I have a score greater than 4 on the Fatigue Severity Scale.
- I have access to a smartphone, tablet, or computer with internet.
- I can understand, read, and speak English.
- I receive cystic fibrosis care at a participating CF Center.
You may not be able to join if
- I have had a lung infection or flare-up in the past 14 days.
- I am pregnant or less than 6 months postpartum.
- I have been advised by my doctor not to engage in light physical activity.
- I participated in the CFWP Feasibility Study.
- I am currently enrolled in another clinical trial.
- I cannot complete coaching sessions within the study timeframe.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
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Answer a few quick questions to see if you may meet the eligibility requirements.
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About This Trial
This study is a pilot randomized control trial (RCT; N=80) comparing the Cystic Fibrosis Wellness Program (CFWP) to usual care (UC) to evaluate (1) Intervention Adherence (completion of the CFWP Coaching Sessions) (2) Study Retention (completion of the Week 15 assessment) and (3) Data Quality (valid daytime and nighttime fitness tracker data). A secondary aim is to gather preliminary data to deter…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. ≥18 years old
2. Documentation of CF diagnosis in the medical record
3. Score of \>4 on the Fatigue Severity Scale
4. Access to a smartphone, tablet, and/or computer with access to internet
5. Ability to understand/read/speak English
6. Receives CF care at a participating CF …
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