Cystic Fibrosis in Children Clinical Trial
Official title:
DESIGN CF: Developing e-Health Systems to Improve Growth and Nutrition in CF Phase 2
Being at or above the 50th percentile body mass index (BMI) for age and gender in children with cystic fibrosis (CF) is associated with better lung functioning as measured by FEV1, yet diet is one of the least adhered to components of the CF treatment regimen. Investigators at Cincinnati Children's Hospital Medical Center (CCHMC) have developed an efficacious behavioral plus nutrition education program (Be In Charge) that improves adherence to dietary recommendations, and promotes weight gain in children with CF. To make Be In Charge (BIC) widely available to families of children with CF ages 3 to 10 years, the investigators translated the face-to-face intervention into a 10-week, web-based intervention (BeInCharge.org). The investigators tested it in a pilot study and the results were promising. In the first phase of the current study, the investigators worked with a team of clinicians, parents and technology developers to extend the usability and functionality of the web intervention, enable parent-clinician collaboration, and support concurrent use across multiple clinical sites. The long term goal of this research is to make BeInCharge.org available through CF Centers across the country to patients that would benefit in order to improve dietary adherence. The current phase of this protocol is a prospective, multicenter, nonrandomized study enrolling up to 150 parents of children with CF. Participants will complete the Be In Charge program outside of CF clinic on their own time. CF Center clinicians will be able to follow the participant's progress via the Be In Charge clinician dashboard. CF center clinicians will be asked to support participating families in completing the program as clinically appropriate. The primary study objective is to: 1. Demonstrate preliminary effectiveness on weight and calorie intake outcomes when the Be In Charge program is integrated into clinical care with implementation support for care teams. The secondary study objectives are to: 1. Develop a well-defined, tested set of implementation strategies consolidated into a change package and an optimized technology platform that will support a dissemination trial for spreading the Be In Charge program across CF Centers. 2. Demonstrate that it is feasible and acceptable to use the Be In Charge program in clinical care and with fidelity to intervention parameters. 3. Demonstrate sustainability of the Be In Charge program through effective use by participants and clinicians.
n/a
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03637504 -
Feasibility of a Mobile Medication Plan Application in CF Patient Care
|
N/A | |
Active, not recruiting |
NCT04602468 -
Real World Clinical Outcomes With Novel Modulator Therapy Combinations in People With CF (RECOVER)
|
Phase 4 | |
Completed |
NCT06109675 -
Nutritional Status Assessment of Pediatric Cystic Fibrosis Patients and Effect of Nutrition Education on Nutritional Status
|
N/A | |
Active, not recruiting |
NCT04392544 -
Intestinal Inflammation in CF Patients
|
||
Completed |
NCT04084041 -
Efficacy of Simeox Airway Clearance Therapy in Children With Cystic Fibrosis
|
N/A | |
Not yet recruiting |
NCT03292718 -
Clinical Trial to Assess Influence of MyCyFAPP Use on GI Related QOL in Children With Cystic Fibrosis
|
N/A | |
Not yet recruiting |
NCT05493137 -
Physical Activity Levels of Parents of Children With Cystic Fibrosis- (PHACTS-CF)
|
||
Enrolling by invitation |
NCT06188988 -
Viral Infections and Airway Microbiome in Young Children With Cystic Fibrosis
|
||
Recruiting |
NCT04174664 -
Comparison of Different Functional Capacity Tests in Cystic Fibrosis Patients With Acute Pulmonary Exacerbation
|
||
Completed |
NCT04138589 -
Effect of Lumacaftor/Ivacaftor in Children With Cystic Fibrosis Homozygote for F508del on Small Airway Function
|
||
Completed |
NCT03579173 -
Determinants of Early Cystic Fibrosis Lung Disease
|
||
Recruiting |
NCT05850351 -
Virtual Reality Based Tele-Exercises on Exercise Capacity in Cystic Fibrosis
|
N/A | |
Completed |
NCT04463628 -
Impacts of the Covid-19 Epidemic and Associated Lockdown Measures on the Management, Health and Behaviors of Cystic Fibrosis Patients During the 2020 Epidemic
|
||
Completed |
NCT04835376 -
Percussion Palm Cup: Safety and Usability in Infants and Children With Cystic Fibrosis
|
N/A | |
Completed |
NCT04293926 -
Heart Rate Variability in Children and Adolescents With Cystic Fibrosis
|
N/A | |
Completed |
NCT04987567 -
Effect of Antioxidant Docosahexaenoic Acid (DHA) in Cystic Fibrosis Patients
|
N/A | |
Withdrawn |
NCT04415268 -
Combined Effect of CFTR Protein Modulator Drugs and Exercise in Cystic Fibrosis
|
N/A | |
Not yet recruiting |
NCT06066723 -
19F MRI in Healthy Children and Children With Mild Cystic Fibrosis Lung Disease
|
||
Terminated |
NCT03939065 -
Sensor Augmented Pump (SAP) Therapy for Inpatient CFRD Management
|
N/A | |
Active, not recruiting |
NCT04613128 -
The PROMISE Pediatric Study 6 to 11 Years Old
|