Home Parenteral Nutrition Clinical Trial
Official title:
Prevention of Home Parenteral Nutrition (HPN) Infection, Depression and Improving Caregiving Problem Solving
The purpose of this study is to help people with home parenteral nutrition (HPN) to avoid infections and feelings of depression or fatigue and to test how their health and quality of life change over time. Another purpose is to test the nurse teaching sessions and the method of obtaining support from the peer partner through videophone.
Aim #1 Hypothesis
1. Dyad (patient-caregiver) participation in health care management and problem-solving
method use with professionals will be greater in the experimental group than the
control group
2. Dyad reactive depression will be lower in the experimental group than the control group
3. Dyad quality of life will be higher in the experimental group than the control group
4. Dyad health status scores will be higher and the dyad sleepiness scale will be lower in
experimental group than the control group
5. Dyad Health Services Use will be lower in the experimental group than the control group
6. Catheter-related infections will be lower in the experimental than control patients
Aim #2 Hypotheses:
1. What is the cost of using the FamTechCare system compared to traditional care?
2. Is there a difference between efficiency scores of the experimental and control groups
intervention, boosters and relative to dyads long-term health services use at 24
months?
3. What are the relationships among patient outcome variables and caregivers' rating of
virtual nurse caring and caregiver adaption?
4. What are the relationships among use of FamTechCare, dyad participation in health care
management scale score and dyad access to the Internet Weighted Score?
;
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Prevention
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05048030 -
Survey of Lifestyle and Its Feelings in Families of Patients in Home Parenteral Nutrition
|
||
Completed |
NCT02009189 -
Taurolidine Lock in Long Term Parenteral Nutrition
|
Phase 4 | |
Completed |
NCT02796833 -
Comparison of Two Intravenous Lipid Emulsions in Home Parenteral Nutrition Patients
|
Phase 4 | |
Withdrawn |
NCT03054948 -
SMOFLipid in Patients Who Are Intralipid Intolerant
|
Phase 4 | |
Completed |
NCT01946503 -
Infant & Toddler Short Gut Feeding Outcomes Study
|