Internet-delivered Cystic Fibrosis Mental Health Prevention, Wellness, Resource Program: How Does it Work? (NCT06020274)
Internet-delivered Cystic Fibrosis Mental Health Prevention, Wellness, Resource (iCF-PWR) Program: How Does it Work?
🩺 Plain-English Summary (8th-Grade Level)
The goal of the clinical trial is to test whether a mental health program that is delivered through the Internet works well for children and adolescents with cystic fibrosis (CF) and their healthy siblings. The main questions it aims to answer are: * Does the program improve the mental health such as depression and anxiety symptoms? * Does the program improve overall quality of life? * Does the program improve self-efficacy - an individual's belief in their ability to complete tasks to achieve their goals? Participants will: * Fill out an online survey asking questions about their personal and health information, as well as their mental health before the program * Complete the online mental health program * Fill out an online survey asking questions about their mental health after completing the program, and 1-month and 3-months following completing the program Participants be compared against another group of children with CF and their healthy siblings who are on a waitlist and receiving usual CF treatment. Researchers will compare participants scores before starting the program with their scores immediately following completing the program, 1-month, and 3-month after completing the program. Researchers hope to develop a program that improves mental health, quality of life, self-efficacy, and knowledge about CF.
Who can join: Review the eligibility criteria below.
Location: BC Children's Hospital — Vancouver, British Columbia
Age range: 8 Years to 12 Years
🧪 Interventions in This Study
- Internet-delivered Cystic Fibrosis Mental Health Prevention, Wellness, and Resource (iCF-PWR) program (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (2 Sites)
- BC Children's Hospital — Vancouver, British Columbia
- Saskatchewan Health Authority — Regina, Saskatchewan
📞 Contact the Study Coordinator
Phone: (306) 550-6874
Email: shivak3s@uregina.ca
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Cystic Fibrosis in Children
- Intestinal Inflammation in CF Patients — Toronto, Ontario
- 19F MRI in Healthy Children and Children With Mild Cystic Fibrosis Lung Disease — Chapel Hill, North Carolina
- Feasibility of Cough Monitoring in Children — Aurora, Colorado
- Sinus Disease in Young Children With Cystic Fibrosis — Aurora, Colorado
- Detection of Unsuspected Small Airways Obstruction in Cystic Fibrosis — Lakewood, California
Explore by condition: All Cystic Fibrosis in Children clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.