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CompletedNCT02320513IAMUpdated Oct 1, 2015

A Comparison of Physical Activity Levels With and Without Feedback Via Fitbit® Flex™ in Hemodialysis Patients

An observational study in End Stage Renal Disease, sponsored by Renal Research Institute. Completed at 1 site in United States. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2015-10-01.

Sponsored by Renal Research Institute · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
33
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This is a pilot study intended to gather data in order to inform future studies about the role of feedback as an incentive for increasing levels of physical activity which could improve health in hemodialysis patients.

Read the detailed description

In prior studies that have analyzed physical activity in dialysis patients, three-dimensional accelerometers, physical performance tasks or self-reporting physical activity questionnaires have been used to measure levels of activity. This proposed study differs in that it will determine the effectiveness of providing "feedback" to dialysis patients using a fitness tracking bracelet. For the purpose of this study, the word 'feedback' is used to refer to the information provided to the subject that demonstrates the number of steps taken since the previous dialysis session as displayed by the Fitbit® application. This 'feedback' will allow subjects to be more aware of their overall physical activity on a quantitative level.

The study will seek to explore an association between feedback and physical activity. Improved physical activity could improve indicators of subjects' health status such as blood pressure, inflammatory markers, and pre-albumin levels, which will also be monitored and recorded.

While informing subjects quantitatively about their levels of physical activity could be a promising method to encourage them to be more active, it is unclear at this point if that strategy actually works. This is an important practical question though, because actually informing subjects on a regular basis about their activity level may pose substantial operative challenges and result in additional costs.

The importance of encouraging subjects to be more physically active should not be underestimated. Studying the physical activity of dialysis patients is important because it allows researchers to consider the long-term effects that may influence the subject's well-being. Johansen et al. showed that there was a direct relationship between the inactivity of dialysis patients and susceptibility to hypertension, diabetes, cardiovascular disease and even mortality. Additionally, the study demonstrated the importance of implementing programs to promote physical activity [1]. If feedback does indeed increase physical activity, then it will be substantially beneficial for this program to be implemented.

02

Conditions studied

  • End Stage Renal Disease

Keywords

  • Exercise
03

In context

Kidney Failure, Chronic

2,085 studies on the registry are indexed under Kidney Failure, Chronic; 260 are open to participants now.

This study's enrollment of 33 is below the median of 120 across 431 observational studies indexed under Kidney Failure, Chronic.

Browse Kidney Failure, Chronic studies →

Lead sponsor

Renal Research Institute is the lead sponsor of 18 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

  • Receiving hemodialysis three times a week
  • On hemodialysis for more than 3 months
  • Between the ages of 18 and 75 years
  • Able to walk without assistance or assistive devices
  • Able to read and understand the English language

Inclusion criteria

  • Receiving hemodialysis three times a week
  • On hemodialysis for more than 3 months
  • Between the ages of 18 and 75 years
  • Able to walk without assistance or assistive devices
  • Able to read and understand the English language

Exclusion criteria

Exclusion Criteria:

  • Patient already uses an activity tracker
  • Unstable health: acute infections, congestive heart failure NYHA class 4 and/or unstable angina
  • Hospitalization within the past 3 months for non-access related reasons
  • Known allergies to nickel
  • Unable to physically grip the handheld dynamometer in order to complete the Hand Grip Strength Test
  • Cognitive impairment
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
33 participants (actual)
Patient registry
No

Groups and cohorts

  • Control Group

    Subjects will wear the activity monitoring device to track their activity between dialysis treatments, however, the feedback from the device will not be shared with them.

    Other: Wearing activty monitoring device (Fitbit Flex) · Device: Fitbit Flex

  • Feedback Group

    The feedback from the activity monitoring device will be shared with subjects at each visit.

    Other: Wearing activty monitoring device (Fitbit Flex) · Device: Fitbit Flex

Interventions

  • OtherWearing activty monitoring device (Fitbit Flex)
  • DeviceFitbit Flex
06

What researchers measure

Primary outcomes

  1. The effect of physical activity feedback on physical activity levels.

    Physical activity level will be measured by the number of steps each subject takes. The number of steps each subject takes will be recorded and reported to those in one of the two groups. The study will evaluate whether a subject will begin to walk more steps once s/he is informed about the number of steps s/he is taking.

    Time frame: 5 weeks

07

Study locations

1 site
  • Avantua Upper East Side Dialysis Center
    New York, New York 10065, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 1, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02320513
Lead sponsor
Renal Research Institute
Responsible party
Sponsor
First posted
Dec 19, 2014
Start date
Oct 2014
Primary completion
Jun 2015
Completion
Jun 2015
Last update
Oct 1, 2015

Study contacts

Peter Kotanko, MD
principal investigator · Renal Research Institute

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2015. You cannot join it, but the record below documents what was studied.

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