Skip to content

Swipe Out Stroke (SOS): Feasibility of Using a Consumer Based Electronic Application to Improve Compliance With Weight Loss in Obese Minority Stroke Patients

Swipe Out Stroke (SOS): Feasibility of Using a Consumer Based Electronic Application to Improve Compliance With Weight Loss in Obese Minority Stroke Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02531074
Acronym
SOS
Enrollment
56
Registered
2015-08-21
Start date
2015-01-31
Completion date
2017-06-30
Last updated
2020-08-18

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

Conditions

Stroke

Keywords

Mobile Applications

Brief summary

This pilot study evaluates the use of a mobile application to improve weight loss in obese stroke patients. The investigators hypothesize that acute stroke patients who use the mobile application are more likely to achieve a minimum 5% weight reduction during the critical six months post-stroke, yielding considerable improvement in stroke risk factors.

Interventions

BEHAVIORALMobile Application
BEHAVIORALFood Journal
BEHAVIORALUsual Care

Sponsors

The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. Ischemic or hemorrhagic stroke. 2. Age 18-85 years. 3. African-American or Hispanic. 4. Modified Rankin Scale (mRS) of 0-3. 5. Body Mass Index greater than 30 kg/m2. 6. Currently taking prescription medication for diabetes mellitus, hypertension or hyperlipidemia. 7. Willing to follow a healthy eating pattern and NOT use weight loss medications for the duration of the study. 8. Personal ownership or caregiver ownership of a personal computer, SmartPhone or other SmartDevice (iPhone or Android platform) with Internet access. 9. If patient has alexia, agraphia, acalculia, dementia or blindness - caregiver must be willing to complete the intervention.

Exclusion criteria

1. Pre-existing disability with mRS \> 4. 2. Contraindications to weight loss (planning to become pregnant, history of an eating disorder). 3. Steroid use for suspected vasculitis. 4. Current or recent (past 6 months) participation in a weight loss program or use of weight loss medication.

Design outcomes

Primary

MeasureTime frame
Number of participants with five percent or greater weight loss.Six months

Secondary

MeasureTime frame
Percentage of patients with blood pressure reduction.Six months
Percentage of patients with decrease in serum cholesterol.Six months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026