The effect on fluid restriction adherence by monitoring with the MySleeve device, a randomized controlled trail.

The effect on fluid restriction adherence by monitoring with the MySleeve device, a randomized controlled trail. - MySleeve study.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON42773

Enrollment

Registered

2015-10-09

Start date

2015-07-01

Completion date

Unknown

Last updated

2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

fluid restriction

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Prevalent hemodialysis patients with a dialysis vintage of at least 3 months. - Anuric (defined as a urine output of

Exclusion criteria

Exclusion criteria: - withdrawal of consent - acute intercurrent illness (infection, malignancy, cardiovascular event, uncontrolled diabetes) - physically constrained to use the required devices - mentally unable to use the required devices

Design outcomes

Primary

Measure	Time frame
less IDWG.	—

Secondary

Measure	Time frame
Improved sleep quality measured by the activity tracker. Increased physical activity, measured by the activity tracker. Evaluation of user experience, and possible suggestions of improvemend, of the MySleeve device and the BCM sock at the end of the study.	—

Countries

Netherlands

Outcome results