Randomised trial of a web-based intervention for adherence in cystic fibrosis
- Conditions
- Cystic fibrosisNutritional, Metabolic, Endocrine
- Registration Number
- ISRCTN37959826
- Lead Sponsor
- eeds Teaching Hospitals Trust (UK)
- Brief Summary
2019 Abstract results in https://doi.org/10.1002/ppul.22495 number 697, page 420 (added 28/10/2022)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 99
1. Patients with a diagnosis of CF, attending Leeds Adult CF unit for their complete care
2. Male or female patients age 16 - 60 years old
3. Consecutive volunteers recruited at time of clinical stability [end of in-patient treatment or at out-patient clinic]
4. Patient must be prescribed a minimum of three specified medications (see below) for at least 6 months prior to signing the informed consent form: azithromycin hypertonic saline, TOBI®, Pulmozyme®, pancreatic enzyme replacement therapy, oral antibiotics, fat-soluble vitamins, insulin, inhaled compounded tobramycin, oral nutritional supplements, insulin, AZLI
1. Pregnancy
2. Acceptance on the lung transplant list (note: participation in this study will not delay or exclude patients from being placed on the transplant list in the future or receiving a transplant once enrolled in the study)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method