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OpenTrials
Completed

NCT Number: NCT03072966

Development of Distress Management Algorithms Using Mobile Device Based Health Logs in Breast Cancer Survivors

Distress monitoring is an important issue in cancer survivors. However, conventional distress screening is very difficult to perform. This study investigates the efficacy of wearable device as a tool of distress monitoring in breast cancer survivors.

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Key information

Age range

20 year–60 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Asan Medical Center

Seoul, Korea, 05505, South Korea

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Stage 0-III breast cancer

Exclusion criteria

  • Stage IV breast cancer
  • Breast cancer recurrence or metastasis
  • Severe medical illness

Treatment and study plan

Wearable device (Fitbit Charge HR® or Fitbit Alta ®)

Device

Physical activities will be monitored by wearable device.

Primary outcomes

  1. Efficacy of distress screening of wearable device

    Time frame: 6months

    The results of distress screening questionnaire and patterns of physical activities are going to be compared. The association between those two data will be analyzed. Using data of physical activities, the prediction model of distress will be tested and validated.

Sponsors and collaborators

Lead sponsor

Asan Medical Center

Other

Registry information

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Mar 8, 2017
Registry last updated
Jan 10, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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