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An Observational Prospective Cohort Study Using an Actigraphy Device.

NCT03475433 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2019-04-10

No results posted yet for this study

Summary

This study focuses on whether or not physical activity and sleep quality correlate with the health of prostate and breast cancer patients. The activity data will be acquired using wearable actigraphy devices, which the subjects will wear for the duration of seven days. The sleep quality will be measured using a combination of actigraphy and the mandarin version of the Pittsburgh Sleep Quality Index (PSQI) and the Quality of Life Questionnaire (QLQ). By using this combination, the investigators will not only measure the objective physical activity while the patient is asleep, but also the subjective sleep quality. The questionnaire will also function as control data for the accuracy of the actigraphy device.

This study will recruit approximately 30 breast or prostate cancer patients. The participants will wear a wearable actigraphy device for 7 consecutive days, which will provide accurate and objective movement and sleep data. This data is linked to a unique Identification number (ID), which will be noted in the participant's case report. This case report also contains the participant's information and answers to the questionnaires.

Conditions

  • Neoplasm of Breast (Disorder)
  • Carcinoma of Prostate (Disorder)

Interventions

DEVICE

Actigraphy device

Both groups will receive an actigraphy device that will passively measure their movement data.

Sponsors & Collaborators

  • Ministry of Science and Technology, Taiwan

    collaborator OTHER_GOV

  • University of Seville

    collaborator OTHER

  • Taipei Medical University WanFang Hospital

    collaborator OTHER

  • Taipei Medical University Hospital

    collaborator OTHER

  • Adhera Health, Inc.

    collaborator INDUSTRY

  • Taipei Medical University

    lead OTHER

Principal Investigators

  • Syed Abdul Shabbir, Dr. MD · Associate Professor & Health IT Consultant

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-15
Primary Completion
2018-07-31
Completion
2018-08-31

Countries

  • Taiwan

Study Locations

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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 NCT03475433 on ClinicalTrials.gov