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Completed

NCT Number: NCT03045276

Urological and Renal Disease Engaging Adolescents in Adherence Collaborative Trial

The purpose of this study is to determine the effectiveness of behavioral feedback plus economic incentives to promote treatment adherence among a large diverse population of adolescents and young adults (AYA) with kidney transplant (KT) or spina bifida (SB).

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Key information

Age range

12 year–24 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Children's Healthcare of Atlanta, Atlanta, Georgia, United States

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About this study

The overarching goal of this five-year, phase II, randomized clinical trial is to improve poor long-term health outcomes in both adolescents and young adults (AYA) with either a kidney transplant (KT) or spina bifida (SB), respectively. More specifically, this study will focus on decreasing premature allograft loss in subjects with kidney transplant (KT) due to medication nonadherence and kidney damage in subjects with SB due to urinary non-continence. To achieve these goals, this study will implement a real-time feedback system, Way to Health (WTH), that will provide education and support, increase awareness and incentivize positive health behavior, in addition to standard of care. Further, this study will investigate the mechanisms of behavior change by examining the role of financial incentives, positive feedback and the relationship between the two. The study will compare two cohorts of KT and SB subjects, which will undergo varied levels of financial incentives and positive feedback. Data from KT and SB subjects will be analyzed jointly and separately. This innovative mobile health (mhealth) strategy will improve our current measures of adherence and increase our understanding of factors that influence adherence for two AYA populations, KT and SB subjects, respectively. The study will contribute novel insight to inform the design of future interventions targeting persistence of behavior change and can be used in other centers and for other chronic disease groups.

The study intervention will use the WTH web-based platform to support AYA with KT or SB as they navigate their daily treatment burdens. This will be achieved via bi-directional text messaging, including the sending of reminders and positive feedback by WTH and the messaging of pictures of medication or catheter in hand at time of treatment by the participant. This intervention will assess sustainability of this novel bi-directional messaging system and the impact of providing education and support, increasing awareness and incentivizing positive health behavior in real-time.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males or females age 12-24 years.
  • Kidney Transplant subjects must be greater than 3 months post-transplant.
  • Spina Bifida subjects must be able to perform Clean Intermittent Catheterization (CIC) as part of their treatment.
  • Able to speak and read in English.
  • Willing and able to provide informed assent or consent.
  • Parental/guardian permission (informed consent) if appropriate.

Exclusion criteria

  • Unwilling to participate.
  • Unable to speak or read in English.
  • Unable to provide informed assent or consent.
  • Severe cognitive impairment, as reported by treating team in recruiting clinic.
  • On dialysis.
  • Acquired post-transplant lymphoproliferative disease less than one year prior to enrollment
  • Less than 3 months post-transplant.
  • Unable to perform CIC.
  • Prescribed Immunosuppressive medications once per day.
  • Provider recommendations of CIC once per day

Treatment and study plan

Behavioral Feedback and Economic Incentives: Arm 1

Behavioral

The purpose of this study is to determine the effectiveness of behavioral feedback plus economic incentives to promote treatment adherence among a large diverse population of adolescents and young adults (AYA) with kidney transplants (KT) or spina bifida (SB). In Arm 1, participants will not receive personalized feedback, nor will they receive the "extra" incentive of $10 for meeting their adherence goal.

Behavioral Feedback and Economic Incentives: Arm 2

Behavioral

The purpose of this study is to determine the effectiveness of behavioral feedback plus economic incentives to promote treatment adherence among a large diverse population of adolescents and young adults (AYA) with kidney transplants (KT) or spina bifida (SB). In Arm 2, participants will receive personalized feedback, and an "extra" incentive of $10 for meeting their adherence goal.

Primary outcomes

  1. Mean Percentage of Subjects With Adherence Behavior Greater Than or Equal to 85% From Baseline and Intervention Period (6-month)

    Time frame: baseline to 6 months

    Participants who do not submit the correct number of pictures within the prescribed window of their expected time due for treatment will be counted as non-adherent for that episode of med taking/cathing. The mean percentage of participants who achieved 85% adherence was calculated for each week from baseline (week 1) to the end of the 6 month time point (week 26).

  2. Study Efficacy of Use of Way to Health Portal System

    Time frame: 12.5 months

    Statistical analysis of the number and timing of messages sent to the Way to Health portal as well as how often the participants used the portal will determine study efficacy.

Secondary outcomes

  1. Change in Pressure Per Unit Volume of Bladder of Spina Bifida Subjects

    Time frame: 12.5 months

    Urodynamic studies (UDS) in spina bifida subjects will test the change in bladder wall compliance, i.e. the change in pressure per unit volume of the bladder.

  2. Change in Coefficient of Variation (CV) of Immunosuppressive Drug Levels (Tacrolimus or Sirolimus) Between the Baseline (run-in) and Intervention Period.

    Time frame: baseline and at 6 months

    The difference between the coefficient of variation (CV) of immunosuppressive drug levels in kidney transplant patients at baseline and intervention period (6 months). CV was calculated using the average of three values of immunosuppressive drug levels at each time point. The change was calculated as the difference in mean value between baseline and 6 months.

Other outcomes

  1. Executive Function

    Time frame: 12.5 months

    Behavior Rating Inventory of Executive Function questionnaire will be administered and answers will be analyzed.

  2. Perceived Treatment Barriers - Spina Bifida

    Time frame: 12.5 months

    The Spina Bifida and Cathing Barriers measure will be administered and answers will be analyzed.

  3. Mean Change in Perceived Adherence Behaviors as Measured by the Adolescent Medication Barriers Scale From Baseline to Intervention Period (6 Months)

    Time frame: Baseline to 6 months

    The Adolescent Medication Barrier Scale will be administered to the kidney transplant patients and answers will be analyzed. The Adolescent Medication Barriers Scale (AMBS) endorsement score is the sum of 17 items (rated 1,2,3=0, rated 4 & 5=1). The higher the endorsement score (range of 0-17) indicates that the adolescent perceived themselves as having more barriers to medication adherence.

  4. Change in Self-Efficacy Score From Baseline to Intervention Period (6 Month)

    Time frame: baseline to 6 months

    Self-Efficacy for Managing Chronic Disease 6-Item Scale ranging from 1 (not at all confident) to 10 (totally confident). Total score is the mean of the 6-tems. The higher the score, the more self-efficacy. The outcome measure is the change in score 6 months-baseline.

  5. Treatment Responsibility

    Time frame: 12.5 months

    Allocation of Treatment Responsibility and the Sharing of Spina Bifida Management Responsibilities surveys will be administered and answers will be analyzed.

  6. Change in Disease Knowledge Score From Baseline to Intervention (6 Months)

    Time frame: baseline to 6 months

    The Heart Transplant Knowledge questionnaire, adapted for Kidney Transplant patients, and the Knowledge of Spina Bifida survey will be administered and answers will be analyzed. There are 20 questions, each correct question = 1, each incorrect question =0. The total score ranges from 0-20. The higher the score, the more knowledge the participant has. The outcome measure will measure the change in score from 6 months to baseline.

Sponsors and collaborators

Lead sponsor

Children's Hospital of Philadelphia

Other

Collaborators

  • Ann & Robert H Lurie Children's Hospital of Chicago
  • Boston Children's Hospital
  • Children's Healthcare of Atlanta
  • Children's Mercy Hospital Kansas City
  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  • National Institutes of Health (NIH)
  • Seattle Children's Hospital

Registry information

Acronym: U-REAACT

Important dates

Study start
2017
Primary completion
2022
Study completion
2022
First posted
Feb 7, 2017
Registry last updated
Nov 9, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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