NCT05692323

Brief Summary

The purpose of this study is to assess the use of an exercise program in people with pancreatic cancer.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
11mo left

Started May 2023

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress77%
May 2023Apr 2027

First Submitted

Initial submission to the registry

January 11, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 20, 2023

Completed
4 months until next milestone

Study Start

First participant enrolled

May 15, 2023

Completed
2.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 15, 2025

Completed
6 months until next milestone

Results Posted

Study results publicly available

April 15, 2026

Completed
12 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2027

Expected
Last Updated

April 15, 2026

Status Verified

April 1, 2026

Enrollment Period

2.4 years

First QC Date

January 11, 2023

Results QC Date

March 4, 2026

Last Update Submit

April 13, 2026

Conditions

Keywords

ExercisePrehabilitation

Outcome Measures

Primary Outcomes (1)

  • PREHAB Feasibility

    PREHAB Program feasibility will be measured by tracking participant attendance at PREHAB sessions. PREHAB will be considered feasible if 50% of participants attend at least 60% of scheduled sessions. PREHAB session feasibility is defined as at least 50% of participants attending at least 60% of scheduled sessions

    From Baseline to 3 Months

Secondary Outcomes (1)

  • PREHAB Program Safety

    From Baseline to 3 Months

Study Arms (1)

Supervised Prehabilitation Exercise Program

EXPERIMENTAL
Other: PREHAB

Interventions

PREHABOTHER

6-week supervised PREHAB program. Each week of the program consists of 3 x 1 hour supervised training sessions made up of moderate intensity aerobic training and resistance training. In addition to the supervised sessions, patients will be instructed to accumulate a total of 150 minutes per week of moderate aerobic training at home which is measured by a wrist worn FitBit device.

Supervised Prehabilitation Exercise Program

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Pancreatic cancer diagnosis (any stage)
  • Age ≥ 18 years
  • Independent ambulation and activities of daily living (Discretion of referring/ treating oncologist)
  • Godin-Shephard Leisure-Time Physical Activity Questionnaire score of ≤ 23
  • Physically able to complete functional assessments including 6-minute walk test, hand grip strength, short performance physical battery and performance metrics
  • Answers no to all questions on PAR-Q OR is cleared to participate by their treating oncologist
  • Ability to read, write and understand English
  • Written informed consent obtained from subject and ability for subjects to comply with the requirements of the study
  • Access to a smart device capable of Fitbit syncing and accessing the online Pain portal (www.painguide.com)

You may not qualify if:

  • Has undergone or plans to undergo resection surgery prior to projected completion of PREHAB exercise intervention
  • Current pregnancy
  • Using a pacemaker, implantable cardiac defibrillator, neurostimulator, cochlear implants (removable hearing aids permitted), or other electronic medical equipment, unless the PI deems study participation safe.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cedars-Sinai Medical Center

Los Angeles, California, 90048, United States

Location

MeSH Terms

Conditions

Pancreatic NeoplasmsMotor Activity

Condition Hierarchy (Ancestors)

Digestive System NeoplasmsNeoplasms by SiteNeoplasmsEndocrine Gland NeoplasmsDigestive System DiseasesPancreatic DiseasesEndocrine System DiseasesBehavior

Results Point of Contact

Title
Dr. Philip Chang
Organization
Cedars-Sinai Medical Center

Study Officials

  • Philip Chang, DO

    Cedars-Sinai Medical Center

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Sponsor-Investigator

Study Record Dates

First Submitted

January 11, 2023

First Posted

January 20, 2023

Study Start

May 15, 2023

Primary Completion

October 15, 2025

Study Completion (Estimated)

April 1, 2027

Last Updated

April 15, 2026

Results First Posted

April 15, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations