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2015-08
2018-07
2018-07
168
NCT02900677
National Taiwan University Hospital
National Taiwan University Hospital
INTERVENTIONAL
Developing Prehabilitation Program in Patients With Operable Pancreatic Cancer Perioperatively and Following Surgery
The aims of this three-year study are to: 1. explore the change of fatigue, nutritional status, quality of life and care needs in patients with operable pancreatic cancer perioperatively and following surgery within 3 months. 2. develop and evaluate the effect of patient-centered cancer prehabilitation care program on improving fatigue, nutritional status and quality of life (QOL) in this population.
Develop and evaluate the effect of patient-centered cancer prehabilitation care program on improving fatigue, nutritional status and quality of life (QOL) in this population.
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
| Study Registration Dates | Results Reporting Dates | Study Record Updates |
|---|---|---|
2016-08-24 | N/A | 2016-09-09 |
2016-09-09 | N/A | 2016-09-14 |
2016-09-14 | N/A | 2016-09 |
This section provides details of the study plan, including how the study is designed and what the study is measuring.
Primary Purpose:
Supportive Care
Allocation:
Randomized
Interventional Model:
Parallel
Masking:
Single
Arms and Interventions
| Participant Group/Arm | Intervention/Treatment |
|---|---|
| EXPERIMENTAL: Physical and nutrition program 6 education programs with physical enhancement and nutrition related information for 12 weeks. | BEHAVIORAL: Physical and nutrition program
|
| NO_INTERVENTION: Control usual care |
| Primary Outcome Measures | Measure Description | Time Frame |
|---|---|---|
| Self-report Questionnaire | The questionnaire includes 25 items to assess the physical symptom distresses | Change from baseline physical symptom at 12 months |
| Secondary Outcome Measures | Measure Description | Time Frame |
|---|---|---|
| Self-report Questionnaire | The questionnaire includes 14 items to assess fatigue intensity and duration | Change from baseline fatigue at 12 months |
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
|
Study Contact Name: Shiow-Ching Shun, PHD Phone Number: 886-2-23123456 Email: scshun@ntu.edu.tw |
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.
Ages Eligible for Study:
ALL
Sexes Eligible for Study:
20 Years
Accepts Healthy Volunteers:
This is where you will find people and organizations involved with this study.
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
No publications available
NPCF was founded on May 29, 2009 and is a 501(c)(3) organization. All donations are tax deductible.
The information and services provided by the National Pancreatic Cancer Foundation are for informational purposes only. The information and services are not intended to be substitutes for professional medical advice, diagnosis or treatment. The National Pancreatic Cancer Foundation does not recommend nor endorse any specific physicians, products or treatments even though they may be mentioned on this site.
