Weight Gain
Conditions
Keywords
Hemodialysis, End stage renal disease on dialysis, Fluid intake, Interdialytic weight gain
Brief summary
Methods are needed to help decrease interdialytic weight gains in hemodialysis patients. One potential method for accomplishing this goal is to develop an app for smartphones that allow patients to track their fluid intake throughout the course of the day. NCT 03759847 was designed to test the safety and efficacy of this app. In this protocol, part of the same IRB number, patients with large interdialytic fluid gains (3.5% or greater) will use the app to to determine the association between the interdialytic weight gain and the fluid consumed as recorded by use of the app for each interdialytic period.
Detailed description
In this full scale study, the app will be used to try and influence fluid intake behavior in those patients who are identified to have large fluid weight gains, as defined by a greater than 4% increase in interdialytic weight. There will be two parts to the full scale trial. In the first part of the full scale study, denoted as the active phase, which will last for two months, study participants will be encouraged to use the app on a daily basis and will meet with the study coordinator on weeks 1, 2, 4, 6, and 8 to further assist the participant in decreasing fluid intake between dialysis sessions. In the second portion of the study, denoted as the passive phase, which will last for six months, the patient will use the app and meet with the study coordinator only when requested by the patient. The number of these sessions will be recorded. At the end of the six month passive phase, the participant will meet for the last time with the study coordinator. During each study visit, subjects will be asked to transfer the data from the App to the study coordinator via the data export function of the app.
Interventions
OTHERFluid intake app
Monitor fluid intake and interdialytic weight gain in patients using the fluid app
Sponsors
Danone Global Research & Innovation Center
Wake Forest University Health Sciences
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE
Intervention model description
Comparison of interdialytic weight gain with fluid intake as recorded by fluid app
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Subject, upon briefing of the content of the present study, fully understanding and agreeing to its objective and having given written (dated and signed) informed consent form to take part in the study. * Adult chronic hemodialysis patient who is at least 18 years of age * Average interdialytic fluid gains of 3.5% or greater of body weight for both weekdays and weekends for a 30 day period * Availability of interdialytic weight gains for the 2 month period prior to enrollment into the study * Access to a smartphone for use of the app and comfort with using apps on a regular basis * Access to a smartphone running under either iOS or Android operating systems * Sufficient knowledge and understanding of the English language to use the application available only in English (US) language * Mental capacity to use and understand the fluid management app * Willingness to share intake data collected with the research team
Exclusion criteria
* Scheduled for a living related renal transplant in the next seven months * Hospitalization within 30 days of entry into the study * Current participation in a randomized clinical trial or in the exclusion period of another clinical trial * Vulnerable subjects defined as individuals whose willingness to volunteer in the clinical trial may be unduly influenced by the expectation, whether justified or not, of benefits associated with participation, or of a retaliatory response from senior members of a hierarchy in case of refusal to participate.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Mean intradialytic weight gain | between baseline (pre-app) and the Active phase (months 1 and 2) | Comparison of interdialytic weight change before and during use of the app |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| 25th percentile of intradialytic weight gain | between baseline (pre-app) and the Active phase (months 1 and 2), between baseline (pre-app) and the Passive phase (month 3-8) | — |
| 75th percentile of intradialytic weight gain | between baseline (pre-app) and the Active phase (months 1 and 2), between baseline (pre-app) and the Passive phase (month 3-8) | — |
| Mean intradialytic weight gain | between baseline (pre-app) and the Active phase (months 1 and 2), between baseline (pre-app) and the Passive phase (month 3-8) | — |
| Percentage of days of app usage | the Active phase (months 1 and 2), Passive phase (month 3 through month 8) | — |
| Number of patients who experienced at least 50% increase in fluid intake during app use | the Active phase (months 1 and 2), Passive phase (month 3 through month 8) | Safety evaluation. |
| Number of days of app usage | the Active phase (months 1 and 2), Passive phase (month 3 through month 8) | — |
Countries
United States
Outcome results
None listed