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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01859104
Other study ID # 13-001535
Secondary ID
Status Withdrawn
Phase N/A
First received May 17, 2013
Last updated March 20, 2018
Start date September 2015
Est. completion date March 2017

Study information

Verified date March 2018
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This current study aims to evaluate the efficacy of engagement modules in assisting patients who are candidates for renal and liver transplantation make significant lifestyle modifications. With the help of the Center for Innovation (CFI), a smartphone app (Android and iOS compatible) has been created to assist in both educating and engaging patients to develop and maintain healthy lifestyle modifications. Our goal is to create a cost-effective, smartphone-based platform that serves to not only efficiently educate but to also verify competence and keep our patients engaged.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date March 2017
Est. primary completion date March 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Individuals who are candidates for liver or renal transplant.

2. Individuals who own a smartphone.

3. Individuals who are obese.

Exclusion Criteria:

1. Patients with prior history of bariatric surgery.

2. Patients with active psychiatric disorder.

3. Patients with active tobacco use.

4. Patients with active substance use (alcohol, illicit drugs, etc.)

Study Design


Intervention

Behavioral:
Use of smartphone app


Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Smart Phone App Feasibility The primary objective will be to assess ease and feasibility of use by subjects. They will provide information through questionnaires developed to assess these factors. 3 months
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