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CancerNCT02175823

Health Status Evaluation for Cancer Survivors by Non-intrusive Sensing System

An observational study of Cancer, run by National Taiwan University Hospital at 1 site in Taiwan.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

To improve quality of life of elderly cancer survivors 1. Using physical activity and environmental sensing technology 2. Monitoring physiological indicators of cancer recurrence Analyzing the patient's circadian rhythm, frailty and his/her vital sign. Vital sign includes blood pressure, weight and hrv. 3. Read more about this study

Who is it for?
Ages 65 years and olderHealthy volunteers can take part
Conditions the study is for
Cancer
How many people
40 participants
Where
1 siteTaiwan
Study dates
Jul 2014to Jul 2015
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 65 years and older
  • All sexes
  • Healthy volunteers accepted
  • Older adult

Study population: Elderly cancer survivors

Who may be able to join

  • The clinical pathology and diagnostic imaging to determine the cancer who completed acute treatment, and patients with more than a month recuperating.
  • Over 65 years old.
  • Proficient in Chinese or Taiwanese.
  • Normal cognitive function

Who cannot join

  • No history of cancer
  • Over 65 years old.
  • Proficient in Chinese or Taiwanese.
  • Normal cognitive function

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • National Taiwan University Hospital

    Taipei, Da'an Dist, 106

    Li Chen Fu, +886-2-3366-3558, lichen@ntu.edu.tw

Other trials in Taiwan

About this study

To improve quality of life of elderly cancer survivors

  1. Using physical activity and environmental sensing technology
  2. Monitoring physiological indicators of cancer recurrence
  • Analyzing the patient's circadian rhythm, frailty and his/her vital sign.
  • Vital sign includes blood pressure, weight and hrv.
  1. Collecting the patient information in real time
  • Giving alarm information to the patient, if any special cases our system found.
  • Giving circadian rhythm report to the patient.
  • Giving healthy report to the patient, collected from his/her vital sign.
Conditions
Cancer
Keywords
Cancer survivors, circadian rhythm, Elderly Patients, frailty
Medical subject headings
Neoplasms, Frailty

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Quality of Life

    Measured: Three weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jun 2014 (estimated)
  2. Study startJul 2014
  3. Primary completionJul 2015 (estimated)
  4. Study completionJul 2015 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Ecologic or community
Time perspective
Prospective
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02175823
Sponsor's protocol ID
201401056RIND
Status last verified
Jul 2014
First submitted
25 Jun 2014
Last updated
8 Jul 2014
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Cancer, run by National Taiwan University Hospital at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 8 Jul 2014. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Li Chen Fu (+886-2-3366-3558, lichen@ntu.edu.tw), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Quality of Life (time frame: Three weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Jul 2014.

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