Web-based Aftercare Intervention for Cardiac Patients

NCT01909349 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1000

Last updated 2017-04-19

No results posted yet for this study

Summary

Persons undergoing cardiac rehabilitation often have difficulties transferring the learned health behaviors into their daily routine which decreases their health status. Computer-based tailored interventions have been shown to be effective in increasing physical activity as well as fruit and vegetable consumption. The aim of this study is, to support people in transferring these two learned behavior changes and their antecedents into their daily life after cardiac rehabilitation in Germany, the Netherlands and China. The primary goal of the study is to analyze the effectiveness of a rehabilitation aftercare program with regard to the level of physical activity and nutrition.

Conditions

Interventions

BEHAVIORAL

self-regulation

Web-based support for behavior change regarding physical activity and fruit \& vegetable consumption

Sponsors & Collaborators

  • Maastricht University

    collaborator OTHER
  • Institute of Physical Education and Sports Sciences

    collaborator OTHER
  • Guangdong Provincial People's Hospital

    collaborator OTHER
  • Hong Kong Baptist University

    collaborator OTHER
  • Jacobs University Bremen gGmbH

    lead OTHER

Principal Investigators

  • Sonia Lippke, Prof. Dr. · Jacobs University Bremen

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2015-09-30
Completion
2016-08-31

Countries

  • China
  • Germany
  • Netherlands

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01909349 on ClinicalTrials.gov