Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02987569
Other study ID # STUDY00004067
Secondary ID R01NR015743-01A1
Status Completed
Phase N/A
First received
Last updated
Start date July 2016
Est. completion date June 2020

Study information

Verified date November 2020
Source University of Kansas Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 83
Est. completion date June 2020
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 13 Years to 30 Years
Eligibility 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

Study Design


Intervention

Behavioral:
mConnect plus mobile connections to multidisciplinary professionals & peers
mConnect is the integration of evidence-based HPN interventions delivered via professionally moderated iPad visual meetings with peers, and reinforced by HPN related skill-building games (apps) and iPad music guided short naps.
iPad use plus one mobile connections to multidisciplinary professionals & peers
iPad with a data plan and one professionally moderated iPad visual meeting with peers.

Locations

Country Name City State
United States University of Kansas Medical Center Kansas City Kansas

Sponsors (2)

Lead Sponsor Collaborator
University of Kansas Medical Center National Institute of Nursing Research (NINR)

Country where clinical trial is conducted

United States, 

References & Publications (1)

Nelson EL, Yadrich DM, Thompson N, Wright S, Stone K, Adams N, Werkowitch M, Smith CE. Telemedicine Support Groups for Home Parenteral Nutrition Users. Nutr Clin Pract. 2017 Dec;32(6):789-798. doi: 10.1177/0884533617735527. Epub 2017 Oct 10. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Health Survey SF-12v2 (predicts future health services use). Physical and mental health status from each person's perspective. 7-Item Likert T0 (baseline data collection)
Primary Quality of Life (Cantril Ladder) Ratings of quality of life over time that are sensitive to changes in health. 3-Item Likert T0 (baseline data collection)
Primary Beck Depression Inventory-II (BDI-II) Assesses assess the intensity of depression into alignment with DSM-IV criteria. Each item is a list of four statements arranged in increasing severity about a particular symptom of depression. 21-Item T0 (baseline data collection)
Primary Use of Healthy Living Activities Prompts, health intentions that predict engagement in targeted activities. Intention scale for healthy activities use (iPad discussion sessions, website use including games; mConnect use) 10-Item Likert T2 (month 1-2/mConnect intervention period)
Primary Use of Healthy Living Activities Prompts, health intentions that predict engagement in targeted activities. Intention scale for healthy activities use (iPad discussion sessions, website use including games; mConnect use) 10-Item Likert T3 (month 3-4/mConnect intervention period)
Primary Beck Depression Inventory-II (BDI-II) Assesses assess the intensity of depression into alignment with DSM-IV criteria. Each item is a list of four statements arranged in increasing severity about a particular symptom of depression. 21-Item T3 (4 months: change from T0/baseline)
Primary Health Survey SF-12v2 (predicts future health services use). Physical and mental health status from each person's perspective. 7-Item Likert T3 (4 months: change from T0/baseline)
Primary Quality of Life (Cantril Ladder) Ratings of quality of life over time that are sensitive to changes in health. 3-Item Likert T3 (4 months: change from T0/baseline)
Primary Health Survey SF-12v2 (predicts future health services use). Physical and mental health status from each person's perspective. 7-Item Likert T4 (8 months: change from T3/4 months)
Primary Quality of Life (Cantril Ladder) Ratings of quality of life over time that are sensitive to changes in health. 3-Item Likert T4 (8 months: change from T3/4 months)
Primary Beck Depression Inventory-II (BDI-II) Assesses assess the intensity of depression into alignment with DSM-IV criteria. Each item is a list of four statements arranged in increasing severity about a particular symptom of depression. 21-Item T4 (8 months: change from T3/4 months)
Primary Health Survey SF-12v2 (predicts future health services use). Physical and mental health status from each person's perspective. 7-Item Likert T5 (12 months: change from T4/8 months)
Primary Quality of Life (Cantril Ladder) Ratings of quality of life over time that are sensitive to changes in health. 3-Item Likert T5 (12 months: change from T4/8 months)
Primary Beck Depression Inventory-II (BDI-II) Assesses assess the intensity of depression into alignment with DSM-IV criteria. Each item is a list of four statements arranged in increasing severity about a particular symptom of depression. 21-Item T5 (12 months: change from T4/8 months)
Secondary Preparedness (measures skills needed for independent HPN home care). Ability to manage home-care; low score = needs home care assistance. 8-Item Likert T0 (baseline data collection)
Secondary COOPS Social Support Scale Ratings on having others who help, listen & provide tangible assistance support. 13-Item Likert T0 (baseline data collection)
Secondary Preparedness (measures skills needed for independent HPN home care). Ability to manage home-care; low score = needs home care assistance. 8-Item Likert T3 (4 months: change from T0/baseline)
Secondary COOPS Social Support Scale Ratings on having others who help, listen & provide tangible assistance support. 13-Item Likert T3 (4 months: change from T0/baseline)
Secondary Mobile Care Helpfulness & Willingness-to-Pay Fees for Distance Health. Rating of Helpfulness and willingness to pay for mobile care delivery. 10-Item Likert T4 (8 months)
Secondary Preparedness (measures skills needed for independent HPN home care). Ability to manage home-care; low score = needs home care assistance. 8-Item Likert T4 (8 months: change from T3/4 months)
Secondary COOPS Social Support Scale Ratings on having others who help, listen & provide tangible assistance support. 13-Item Likert T4 (8 months: change from T3/4 months)
Secondary Preparedness (measures skills needed for independent HPN home care). Ability to manage home-care; low score = needs home care assistance. 8-Item Likert T5 (12 months: change from T4/8 months)
Secondary COOPS Social Support Scale Ratings on having others who help, listen & provide tangible assistance support. 13-Item Likert T5 (12 months: change from T4/8 months)
See also
  Status Clinical Trial Phase
Completed NCT04448041 - CRANE Feasibility Study: Nutritional Intervention for Patients Undergoing Cancer Surgery in Low- and Middle-Income Countries
Completed NCT03268902 - Early Life Interventions for Childhood Growth and Development In Tanzania Phase 2/Phase 3
Active, not recruiting NCT04746664 - Effects of Nutrition Counselling on Old Age People's Nutritional Status and Quality of Life in Bahir Dar City, North West Ethiopia N/A
Completed NCT04608656 - Livestock for Health Project N/A
Completed NCT06009198 - Nutritional, and WASH Related Education Intervention to Address Malnutrition of Early Adolescents in Pakistan N/A
Recruiting NCT05417672 - Assessment of Relationship Between Preoperative Nutritional Status and Perioperative/Postoperative Conditions in Patients With Lung Cancer Scheduled for Lobectomy
Recruiting NCT05257980 - Evaluation of Four New Ready to Drink Oral Nutritional Supplements: Adult ONS Trial N/A
Completed NCT03628196 - A Nutrition-Focused QIP in Outpatient Clinics
Completed NCT05015647 - Low Protein Diet in CKD Patients at Risk of Malnutrition N/A
Enrolling by invitation NCT04675229 - Extending the Validation of SCREEN to Persons Living With Dementia or in Retirement Homes
Recruiting NCT04627376 - Multimodal Program for Cancer Related Cachexia Prevention N/A
Not yet recruiting NCT05860556 - Sustainable Eating Pattern to Limit Malnutrition in Older Adults
Not yet recruiting NCT06047054 - Incidence Rate and Risk Factors of Malnutrition in ICU
Not yet recruiting NCT04398836 - Preoperative Nutrition for Crohn's Disease Patients Phase 3
Not yet recruiting NCT04183075 - Impact of a Nutritional Supplement on the Recovery of the Nutritional Status of Patients With Spontaneous Hip Fracture N/A
Not yet recruiting NCT03150927 - Clinical Study of Novel Probiotic Microbial Compositeā„¢ to Treat Undernourished Young Children N/A
Recruiting NCT02833740 - Comparing Performance of Simplified Mid-Upper Arm Circumference Devices ("Click-MUACs") to Detect Acute Malnutrition N/A
Recruiting NCT03408067 - Evaluation of the Efficacy of Nutritional Risk Screening Tests, NRS 2002 and SGA, to Identifying Malnourished Patients N/A
Completed NCT02938234 - Tolerance and Compliance of a High Caloric, High Protein Oral Nutritional Supplement - Free Intake N/A
Completed NCT02938247 - Tolerance and Compliance of a High Caloric, High Protein Oral Nutritional Supplement - Scheduled Intake N/A