Status:

UNKNOWN

The Efficacy of Health Partnership Program for Cancer Patients

Lead Sponsor:

National Cancer Center, Korea

Collaborating Sponsors:

Samsung Medical Center

Seoul National University Hospital

Conditions:

Breast Cancer

Colon Cancer

Eligibility:

All Genders

20+ years

Phase:

NA

Brief Summary

The Objectives of this study is 1. To evaluate the efficacy for exercise, diet, and posttraumatic growth as a result of participating in tailored program (Health Partnership Program) for 24 weeks 2. ...

Detailed Description

\*\*\*Background Improving cancer patients' quality of life has been increasing subject of research for several years. Especially, the patients and their families who are needed to deal with specific...

Eligibility Criteria

Inclusion

  • Adult(≥ 20 years)
  • Within 24 months of completion of primary treatment with curative intent (Surgery, radiotherapy, chemotherapy)
  • Breast, cervical, colorectal (except rectal cancer), lung, and stomach cancer
  • More than two problematic areas among exercise, diet (Fruit \& Vegetable: F\&V), and posttraumatic growth(exercise \< 150min/week, ≥ 3mets, F\&V \< 5/day, PTGI \< 71)

Exclusion

  • Evidence of secondary tumor, metastasis and recurrence
  • Patients undergoing or planning surgery, radiation therapy or chemotherapy
  • Not Korean speaking and reading (Not communication with Korean)
  • Not understanding of the study purpose and not written informed consent
  • Participants who have an similar study experience
  • Major health problem in which exercise/nutrition intervention is contraindicated at the discretion of clinician; cardiovascular disease (congestive heart failure, angina), pulmonary disease (chronic obstructive pulmonary disease, restrictive pulmonary disease), uncontrolled hypertension, poorly controlled diabetes and severe musculoskeletal disease and so on
  • Sign of infection (body temperature ≥ 37.2℃ or WBC ≥ 11,000)
  • Being pregnant
  • Thrombocytopenia (platelet count ≤ 100,000/mcl)
  • Anemia (Hb ≤ 10g/dL)
  • SGOT or SGPT \> 40 IU/L
  • Creatinine \> 1.2 mg/dL
  • Severe psychiatric disorder (psychotic disorder, major depression and so on) or suicidal tendencies
  • dyspnea

Key Trial Info

Start Date :

February 1 2012

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 1 2013

Estimated Enrollment :

248 Patients enrolled

Trial Details

Trial ID

NCT01527409

Start Date

February 1 2012

End Date

June 1 2013

Last Update

February 7 2012

Active Locations (10)

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Page 1 of 3 (10 locations)

1

Seoul National University Boondang Hospital

Boondang, Gyunggi, South Korea

2

National Cancer Center

Goyang, Gyunggi, South Korea

3

Ajou University Medical Center

Suwon, Gyunggi, South Korea

4

Keimyng University Dongsan Center

Daegu, South Korea