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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04300842
Other study ID # N201910036
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date December 22, 2019
Est. completion date December 26, 2021

Study information

Verified date December 2019
Source Taipei Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This project expects to enroll 60 cancer patients, 60 healthy people and their subjective-objective measurements on fatigue, stress, and total steps will be validated so that the information can be used in further care and improvement of life of quality of the patients.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 120
Est. completion date December 26, 2021
Est. primary completion date December 26, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Age ? 20 years old;

- One group had a cancer diagnosis, one group no cancer diagnosis;

- Can continuous wearing bracelet for 5 days or more

Exclusion Criteria:

- Unclear and unable to answer the questionnaire

Study Design


Related Conditions & MeSH terms


Intervention

Device:
smart bracelet
to measure the stress, fatigue, and activity.

Locations

Country Name City State
Taiwan Taipei Medical University Taipei

Sponsors (1)

Lead Sponsor Collaborator
Taipei Medical University

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary fatigue Unit of measure: severity of fatigue level; measurement tool: Brief Fatigue Index over 5 days
Primary Heart Rate Variability (HRV) monitor Use a digital device to measure the heart rate variability and calculate the HRV data over 5 days
Secondary Distress Thermometer(DT) a screening measure to identify and address psychological distress in individuals with cancer. a cutoff score of 3 on the DT to indicate patients with clinically elevated levels of distress. over 5 days
Secondary Leeds Sleep Evaluation Questionnaire(LSEQ) To assess sleep quality, higher scores mean more disrupt sleep. over 5 days
Secondary International Physical Activity Questionnaire(IPAQ) Life activity survey over 5 days
Secondary Perceived Stress Scale (PSS) higher scores mean more stressful condition over 5 days
See also
  Status Clinical Trial Phase
Terminated NCT02970500 - Effect of Methylphenidate on Cancer-related Cognitive Impairment Phase 2
Not yet recruiting NCT04843657 - Precise Care for Cancer Related Fatigue