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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02175823
Other study ID # 201401056RIND
Secondary ID
Status Not yet recruiting
Phase N/A
First received June 25, 2014
Last updated July 3, 2014
Start date July 2014
Est. completion date July 2015

Study information

Verified date July 2014
Source National Taiwan University Hospital
Contact Li Chen Fu
Phone +886-2-3366-3558
Email lichen@ntu.edu.tw
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical 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. 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date July 2015
Est. primary completion date July 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

- 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

Exclusion Criteria:

- No history of cancer

- Over 65 years old.

- Proficient in Chinese or Taiwanese.

- Normal cognitive function

Study Design

Observational Model: Ecologic or Community, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei Da'an Dist

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of Life Three weeks Yes
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