NCT02175823

Brief Summary

To improve quality of life of elderly cancer survivors

  • Analyzing the patient's circadian rhythm, frailty and his/her vital sign.
  • Vital sign includes blood pressure, weight and hrv.
  • 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jul 2014

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 25, 2014

Completed
1 day until next milestone

First Posted

Study publicly available on registry

June 26, 2014

Completed
5 days until next milestone

Study Start

First participant enrolled

July 1, 2014

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2015

Completed
Last Updated

July 8, 2014

Status Verified

July 1, 2014

Enrollment Period

1 year

First QC Date

June 25, 2014

Last Update Submit

July 3, 2014

Conditions

Cancer

Keywords

Cancer survivorscircadian rhythmElderly Patientsfrailty

Outcome Measures

Primary Outcomes (1)

  • Quality of Life

    Three weeks

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)
Sampling MethodProbability Sample
Study Population

Elderly cancer survivors

You may qualify if:

  • 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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Taiwan University Hospital

Taipei, Da'an Dist, 106, Taiwan

Location

MeSH Terms

Conditions

NeoplasmsFrailty

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Li Chen Fu

    Computer Science and Information Engineering

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Li Chen Fu

CONTACT

+886-2-3366-3558lichen@ntu.edu.tw

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 25, 2014

First Posted

June 26, 2014

Study Start

July 1, 2014

Primary Completion

July 1, 2015

Study Completion

July 1, 2015

Last Updated

July 8, 2014

Record last verified: 2014-07

Locations

TW(1)