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NCT03951363: iControl CKD

iControl Chronic Kidney Disease

Terminated NA Last updated 18 February 2021
What this trial tests

NA trial testing interactive Obesity Treatment Approach (iOTA) in Chronic Kidney Diseases in 4 participants. Terminated before completion.

Timeline
13 May 2019
Primary endpoint
20 February 2020
20 February 2020

Quick facts

Lead sponsorDuke University
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment4
Start date13 May 2019
Primary completion20 February 2020
Estimated completion20 February 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Duke University

Who can join

18 and older, any sex, with Chronic Kidney Diseases. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The proposed study is responsive to the call for obtaining enhanced preliminary data for an external grant resubmission. The goal is to demonstrate a novel approach using digital health tools to help preserve kidney function. The investigators aim to adapt a previous behavioral intervention and conduct formative testing among patients with CKD. Specifically, the investigators will: Aim 1: Modify an existing technology platform to build the iControl CKD system and adapt intervention content to reflect behavioral guidelines for patients with mild to moderate CKD. Aim 2: Conduct qualitative interviews and user testing among patients with CKD to obtain feedback on the design of the intervention. Aim 3: Conduct a prospective cohort feasibility trial to assess the feasibility and initial acceptability of the iControl CKD intervention.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Chronic Kidney Diseases

Currently open trials in the same condition.

Other Duke University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing