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Developing Prehabilitation Program in Patients With Operable Pancreatic Cancer Perioperatively and Following Surgery

Developing and Testing the Effects of Patient-centered Prehabilitation Program on Improving Fatigue, Nutritional Status, and Quality of Life in Patients With Operable Pancreatic Cancer Perioperatively and Following Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02900677
Enrollment
168
Registered
2016-09-14
Start date
2015-08-31
Completion date
2018-07-31
Last updated
2016-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic Cancer

Keywords

Pancreatic Cancer, Fatigue, Nutrition, Quality of Life

Brief summary

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.

Detailed description

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.

Interventions

BEHAVIORALPhysical and nutrition program

6 education programs with physical enhancement and nutrition related information for 12 weeks

Sponsors

National Science and Technology Council, Taiwan
CollaboratorOTHER_GOV
National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* patients with pancreatic cancer and are going to receive surgery.

Exclusion criteria

* poor functional status

Design outcomes

Primary

MeasureTime frameDescription
Self-report QuestionnaireChange from baseline physical symptom at 12 monthsThe questionnaire includes 25 items to assess the physical symptom distresses

Secondary

MeasureTime frameDescription
Self-report QuestionnaireChange from baseline fatigue at 12 monthsThe questionnaire includes 14 items to assess fatigue intensity and duration

Other

MeasureTime frameDescription
Self-report QuestionnaireChange from baseline quality of life at 12 monthsThe questionnaire includes 32 items to assess quality of life

Countries

Taiwan

Contacts

Primary ContactShiow-Ching Shun, PHD
scshun@ntu.edu.tw886-2-23123456

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026