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Televideo Exercise and Nutrition Program for Kidney Transplant Recipients

University of Kansas logo

University of Kansas

Status

Completed

Conditions

Physical Activity
Kidney Transplant Recipient
Diet Modification

Treatments

Behavioral: Televideo Lifestyle Coaching
Behavioral: Enhanced Usual Care

Study type

Interventional

Funder types

Other

Identifiers

NCT03697317
STUDY00140695

Details and patient eligibility

About

The improvement in morbidity and mortality observed with kidney transplantation is often curtailed by post-transplant weight gain, which is common among kidney transplant recipients (KTR). Post-transplant weight gain is associated with serious health issues such as cardiovascular disease, new onset diabetes after transplantation, and graft failure. Although these adverse effects of post-transplant weight gain are well recognized, interventions that target the modifiable risk factors of diet and physical activity to address post-transplantation weight gain are lacking. The purpose of this study is to test the feasibility of an in-home, televideo health coaching to increase the healthy behaviors of KTRs who are 6 months post-transplantation.

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 years or older
  • Between 6 and 12 months post kidney transplantation
  • Kidney allograft only
  • Functioning allograft (not on dialysis)
  • BMI ≥ 22 kg/m2
  • Available to participate in assessments over 6 months
  • Ability to speak and understand English
  • Able to report data weekly by at least one of three alternative methods: telephone, email, or fax
  • Access to wireless internet

Exclusion criteria

  • Multi-organ transplant recipient
  • Uncontrolled diabetes (Hemoglobin A1c≥8%)
  • Currently pregnant or planning on becoming pregnant during the study
  • Participation in a formal weight management, nutrition, or physical activity program
  • Diagnosis of a major psychiatric illness
  • Major dietary restrictions
  • Inability to perform moderate to vigorous physical activity
  • Unwillingness to be randomized
  • Receiving supplemental nutrition

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

10 participants in 2 patient groups

Televideo Lifestyle Coaching
Experimental group
Treatment:
Behavioral: Televideo Lifestyle Coaching
Enhanced Usual Care
Active Comparator group
Treatment:
Behavioral: Enhanced Usual Care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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