Completed
STimulating ImProved Health And Well-being In CysTic Fibrosis Using Integration Of Fitness Technology and Port CF.
What is being collected
Data Collection
Collected from today forward - ProspectiveWho is being recruted
Cystic Fibrosis+5
+ Digestive System Diseases
+ Infant, Newborn, Diseases
From 18 to 100 Years
+6 Eligibility Criteria
How is the trial designed
Case-Only
Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.Observational
Study Start: September 2019
Summary
Principal SponsorMedical College of Wisconsin
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner
Study start date: September 10, 2019
Actual date on which the first participant was enrolled.Cystic fibrosis patients who are willing to use an activity tracker for 3 months are invited to participate. Analysis of activity patterns and sleep patterns will be analyzed and compared to their lung function and general health as part of the routine CF center care visits during the study period.
Official TitleSTimulating ImProved Health And Well-being In CysTic Fibrosis Using Integration Of Fitness Technology and Port CF.
Principal SponsorMedical College of Wisconsin
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
21 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-only
These studies focus only on individuals who have a specific disease. Researchers examine patterns—often genetic or environmental—to uncover what might be linked to the condition.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Any sex
Biological sex of participants that are eligible to enroll.From 18 to 100 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Cystic FibrosisDigestive System DiseasesInfant, Newborn, DiseasesLung DiseasesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesPancreatic DiseasesRespiratory Tract DiseasesGenetic Diseases, Inborn
Criteria
2 inclusion criteria required to participate
Adults with Cystic Fibrosis
Age >18, Cystic Fibrosis
4 exclusion criteria prevent from participating
A potential subject who meets any of the following exclusion criteria is ineligible to participate in the study.
Those unable to commit to at least 3 months follow up for CF care from enrollment at study CF center. Inability to speak and understand English.
Those patients without dedicated access to a smartphone, tablet, or computer with internet for syncing device and completing patient diary.
Those patients unwilling to sign an informed consent form.
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Suspended
Medical College of Wisconsin/Froedtert Hospital
Milwaukee, United StatesOpen Medical College of Wisconsin/Froedtert Hospital in Google MapsCompletedOne Study Center