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A randomized trial for the beneficial effect of pre-operative intervention on physical frailty as a poor prognostic factor after surgery for gastrointestinal cancer in older adults

A randomized trial for the beneficial effect of pre-operative intervention on physical frailty as a poor prognostic factor after surgery for gastrointestinal cancer in older adults - A trial for the beneficial effect of pre-operative intervention in older adults with gastrointestinal cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000024526
Enrollment
100
Registered
2016-12-01
Start date
2017-08-28
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

gastrointestinal cancer

Interventions

Intervention Group:intervention with physical training and amino acids replenishment Control group:without intervention

Sponsors

Geriatric and General Medicine, Gastroenterological surgery, Osaka University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) the ambulatory patients aged 70 years or older in Osaka University Hospital expecting to undergo digestive operations for gastrointestinal cancers (e.g. stomach/duodenum, esophagus, colorectal, hepatic, gallbladder, bile duct, and pancreas) within stage 3 2) the subjects diagnosed as physical frailty (decline of grip strength and/or gait speed)

Exclusion criteria

Exclusion criteria: 1) the subjects with effort angina, chronic heart failure and tachyarrhythmia 2) the subjects with chronic respiratory failure 3) the subjects with active multiple cancers 4) the subjects who undergo preoperative chemotherapy 5) the subjects not able to walk by themselves 6) the subjects with chronic kidney disease 7) the subjects with severe hepatic dysfunction 8) the subjects with cognitive impairment 9) the subjects participating other clinical investigations

Design outcomes

Primary

MeasureTime frame
postoperative complications

Secondary

MeasureTime frame
1) prognosis 1 year after surgery 2) changes of values of comprehensive geriatric assessment (CGA) 3) changes of body composition 4) changes of physical functions 5) changes of several biochemical tests 6) changes of serum concentrations of myokines and vitamin D

Countries

Japan

Contacts

Public ContactHiroshi Akasaka

Osaka University Graduate School of Medicine Osaka University Graduate School of Medicine

akasaka@geriat.med.osaka-u.ac.jp06-6879-3852

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026