Teen and Young Adult Connections for Support From Multidisciplinary Professionals & Peers



Status:Active, not recruiting
Conditions:Food Studies, Gastrointestinal, Nephrology
Therapuetic Areas:Gastroenterology, Nephrology / Urology, Pharmacology / Toxicology
Healthy:No
Age Range:13 - 30
Updated:2/20/2019
Start Date:July 2016
End Date:December 2019

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Teen Connections for Support From Multidisciplinary Professionals & Peers

12 month study testing mobile delivery of health information and connections to professionals
and peers to improve health of teen/young adult HPN users.

This research study will test the effect of in-home/mobile HPN support delivered to teen and
young adult home parenteral nutrition (HPN) patients and family members over handheld
personal computers. Effects on health status, QoL, and fatigue will be assessed over time
between groups of study subjects from the ages of 13 through 30 randomized to one of two
groups. Group One (intervention group) will receive mConnect, integrated evidence-based
interventions (skill-building games, restorative naps & peer support) via mobile iPad and
Internet delivery plus two real-time audiovisual encrypted connections with multidisciplinary
professionals and peers. Group Two (control group) will receive healthy activity information
via mobile iPad and Internet delivery plus one real-time audiovisual encrypted connection
with professionals and peers.

Inclusion Criteria:

- Total parenteral nutrition (TPN) patients/users and family members/caregivers (defined
as those individuals involved in daily home HPN care) age 13 and older

- TPN users (also called HPN users) ages 13 through 30 must be receiving intravenous
nutrition for a non-malignant short bowel disorder

- Read, write, speak English and provide informed consent

- Be able to participate in group clinic visits

Exclusion Criteria:

- Enteral nutrition dependency only

- Less than 13 years of age

- 13 through 17 years of age without parental consent

- Currently enrolled in an intervention study or HPN management program

- Severe cognitive impairment

- Disability disorders (e.g. blindness which cannot be accommodated for active
participation in the group clinics
We found this trial at
1
site
3901 Rainbow Blvd
Kansas City, Kansas 66160
(913) 588-5000
Principal Investigator: Carol Smith, RN, PhD, FAAN
University of Kansas Medical Center The University of Kansas Medical Center serves Kansas through excellence...
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mi
from
Kansas City, KS
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