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Randomised trial of a web-based intervention for adherence in cystic fibrosis

Not Applicable
Completed
Conditions
Cystic fibrosis
Nutritional, 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
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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