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Clinical Trials/NCT02812082
NCT02812082
Withdrawn
N/A

Developing and Assessing the Feasibility of Implementing a Video Web-based Patient Education Application

Memorial Sloan Kettering Cancer Center1 site in 1 countryJune 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Allo-SCT Patients
Sponsor
Memorial Sloan Kettering Cancer Center
Locations
1
Primary Endpoint
Percentage of patients that use the application
Status
Withdrawn
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to develop an interactive web-based patient education program to help educate patients about the increased risk of MS and its cardiac risk factors following allo-SCT and to inform and motivate patients how to make lifestyle changes. This program will be used in addition to counseling at participants clinic visits. The investigators are not changing the recommendations for prevention and management of these conditions, but rather are trying to improve the way they provide this education to patients.

Registry
clinicaltrials.gov
Start Date
June 2016
End Date
June 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • The option to participate will be offered to male and female allo-SCT patients at MSK ≥ 21 years of age who are greater than 90 days post-transplant and followed in or referred to the adult allo-SCT survivorship clinic at MSK
  • The option to participate will be offered to male and female allo-SCT patients at MSK ≥ 21 years of age who are greater than 90 days post-transplant and disease free, but have not yet been referred to the survivorship clinic
  • Able to understand written and oral English

Exclusion Criteria

  • Patients less than 90 days post-transplant
  • Patients without internet access
  • Adult post-transplant patients who have relapsed prior to study recruitment

Outcomes

Primary Outcomes

Percentage of patients that use the application

Time Frame: 1 year

A successful trial will be when ≥ 50% of enrolled patients use the application.

Study Sites (1)

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