search
Back to results

PancFit: Multimodal Exercise During Preoperative Therapy for Pancreatic Cancer

Primary Purpose

Other Disorders of Glucose Regulation and Pancreatic Internal Secretion, Pancreatic Cancer

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Questionnaires
Nutritional Questionnaire and Nutritional Counseling
Booklet
Aerobic Exercise and Strength Training Exercises
Phone Calls
Physical Assessments
Sponsored by
M.D. Anderson Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Other Disorders of Glucose Regulation and Pancreatic Internal Secretion focused on measuring Other disorders of glucose regulation and pancreatic internal secretion, Pancreatic cancer, Questionnaires, Surveys, Nutritional Questionnaire, Nutritional Counseling, Booklet, Pamphlet, Educational materials, Aerobic Exercise, Strength Training Exercises, Physical Assessments, Walk Test

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Pancreatic cancer of any type, biopsy-proven
  2. Scheduled to receive preoperative therapy (chemotherapy, radiation or chemoradiation) either on- or off-protocol.
  3. Anticipated to undergo pancreatectomy in >/= 6 weeks from enrollment
  4. Able to understand the description of the study and willing to participate
  5. Able to understand the exercise program
  6. Able to maintain daily exercise logs
  7. Telephone or email access and agreement to engage with the research personnel via phone or email
  8. Meet all screening requirements.

Exclusion Criteria:

  1. Non-English speaking
  2. Unable to complete the baseline assessment questionnaires or functional assessments
  3. Underlying unstable cardiac or pulmonary disease or symptomatic cardiac disease (New York Heart Association functional class III or IV)
  4. Recent fracture or acute musculoskeletal injury that precludes the ability to weight bear fully on all 4 limbs in order to participate in an exercise intervention
  5. Numeric pain rating scale of >/= 7 out of 10
  6. Myopathic or rheumatologic disease that impacts physical function
  7. Recurrent cancer following prior resection
  8. Neuroendocrine cancer
  9. Completed preoperative therapy and are on their presurgical rest period.

Sites / Locations

  • University of Texas MD Anderson Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Arm A: Standard of Care (SOC)

Arm B: Multi-Modal Exercise and Nutrition Program (MMENP)

Arm Description

After completion of chemotherapy and/or radiation, 3-6 weeks after surgery, and then 3-7 months after surgery: Participants complete 4 questionnaires about physical abilities, motivation, and quality of life. Participant's hand grip strength measured. Participants arm strength measured using an arm curl test. Participants asked to rise from a chair without using their arms to push off. Participants complete a 6-minute walk test to see how far participant can walk in 6 minutes. Participants complete a nutritional questionnaire and receive nutritional counseling. Participants receive educational materials and personalized counseling based on participant's answers. Participants encouraged to remain active during chemotherapy and/or radiation. Participants receive a booklet that contains a stretching guide with full-body stretches and safety.

After completion of chemotherapy and/or radiation, 3-6 weeks after surgery, then 3-7 months after surgery: Participants complete 4 questionnaires about physical abilities, motivation, and quality of life. Participant's hand grip strength measured. Participants arm strength measured. Participants asked to rise from a chair without using their arms to push off. Participants complete a 6-minute walk test to see how far participant can walk in 6 minutes. Participants complete a nutritional questionnaire and receive nutritional counseling. Participants receive educational materials and personalized counseling based on participant's answers. Participants complete moderate-intensity aerobic exercise 5 days each week. Participants complete strength training exercises 2 times per week. Participants contacted by phone by member of study staff 1 time each week for the first 4 weeks, and then every 2 weeks after that for behavioral skills training and to see how participant is doing.

Outcomes

Primary Outcome Measures

Change in 6 Minute Walk Test (6MWT)
Primary endpoint is the change in 6MWT distance, measured in meters, between the time at which preoperative therapy is administered (T0) and the time at which it ends (T1).

Secondary Outcome Measures

Full Information

First Posted
June 13, 2017
Last Updated
October 6, 2023
Sponsor
M.D. Anderson Cancer Center
search

1. Study Identification

Unique Protocol Identification Number
NCT03187951
Brief Title
PancFit: Multimodal Exercise During Preoperative Therapy for Pancreatic Cancer
Official Title
PancFit: Multimodal Exercise During Preoperative Therapy for Pancreatic Cancer: A Randomized Trial Testing Effects on Fitness, Health-Related Quality of Life, and Tumor Vasculature
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 13, 2017 (Actual)
Primary Completion Date
December 31, 2022 (Actual)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
M.D. Anderson Cancer Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Any time the words "you," "your," "I," or "me" appear, it is meant to apply to the potential participant. The goal of this clinical research study is to learn if regular exercise and behavioral skills training can help to improve physical activity in patients with pancreatic cancer who are scheduled to receive chemotherapy and/or radiation before standard-of-care surgery. This is an investigational study. Up to 128 participants will be enrolled on this study. All will take part at MD Anderson.
Detailed Description
Study Groups: If you are found to be eligible to take part in this study, you will be randomly assigned (as in the flip of a coin) to 1 of 2 study arms. This is done because no one knows if one study arm is better than, the same, or worse than the other group. If you are in Arm A, you will not take part in a structured exercise program. If you are in Arm B, you will take part in a structured exercise program and behavioral skills training as described below. Length of Study: You will continue to take part in this study for up to 7 months after your scheduled standard-of-care surgery. However, if intolerable side effects occur or the disease appears to get worse, the study staff will decide if continuing the exercise program is in your best interest. Study Visits: At your baseline visit, after you complete chemotherapy and/or radiation, 3-6 weeks after surgery, and then 3-7 months after surgery: You will complete 4 questionnaires about your physical abilities, motivation, and quality of life. They should take about 25 minutes total to complete. Your hand grip strength will be measured using a hand-held machine Your arm strength will be measured using an arm curl test. You will be given a small weight (about 5-8 pounds) and asked to perform as many bicep curls as you can for 30 seconds. You will be asked to rise from a chair without using your arms to push off. You will complete a 6-minute walk test to see how far you can walk in 6 minutes. You will complete a nutritional questionnaire and receive nutritional counseling. The questionnaire will ask about your diet and any recent weight loss. It should take about 5 minutes to complete. After you complete the questionnaire, you will receive educational materials and personalized counseling based on your answers. If you are in Arm B, you will receive behavioral skills training to teach you ways to monitor your health, set goals, and reward yourself. It should take about 15 minutes to complete. At the baseline visit, you will be given a Fitbit Charge 2 activity tracker to wear during the study. This is a small device designed to record your physical activity and sleep during the study. This device will allow you to monitor your own physical activity and sleep and may help you achieve your goals. You can keep the Fitbit after the study is over. If you are in Arm B, one (1) time each week for the first 4 weeks and then every 2 weeks after that, a member of the study staff will contact you by phone for behavioral skills training and to see how you are doing. These calls should last about 15 minutes. For 2 weeks during each phase of chemotherapy and/or radiation you receive, you will wear a small activity monitor on an elastic band. This will be worn in addition to your Fitbit. Exercise Programs: ARM A: If you are in Arm A, you will be encouraged to remain active during chemotherapy and/or radiation, but you will not receive instruction about aerobic or strengthening exercises. You will receive a booklet that contains a stretching guide with full-body stretches and safety. ARM B: If you are in Arm B, you will be asked to complete up to 30 minutes of moderate-intensity aerobic exercise (such as brisk walking, stationary cycling, and/or elliptical or stair stepping machines) for at least 5 days each week. You will also complete strength training exercises at least 2 times per week. You will complete 1 set of 10-15 repetitions for each of the 8 exercises that you are taught. Over time, the amount of resistance, repetitions, and/or sets may increase or decrease based on your strength. You will be given 5 different resistance tubes to complete these exercises, but you may use free-weights or machines if you prefer. You should complete warm up exercises and 5 minutes of stretching before and after strength training. You must keep a daily activity log to document your exercises.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Other Disorders of Glucose Regulation and Pancreatic Internal Secretion, Pancreatic Cancer
Keywords
Other disorders of glucose regulation and pancreatic internal secretion, Pancreatic cancer, Questionnaires, Surveys, Nutritional Questionnaire, Nutritional Counseling, Booklet, Pamphlet, Educational materials, Aerobic Exercise, Strength Training Exercises, Physical Assessments, Walk Test

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
152 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm A: Standard of Care (SOC)
Arm Type
Experimental
Arm Description
After completion of chemotherapy and/or radiation, 3-6 weeks after surgery, and then 3-7 months after surgery: Participants complete 4 questionnaires about physical abilities, motivation, and quality of life. Participant's hand grip strength measured. Participants arm strength measured using an arm curl test. Participants asked to rise from a chair without using their arms to push off. Participants complete a 6-minute walk test to see how far participant can walk in 6 minutes. Participants complete a nutritional questionnaire and receive nutritional counseling. Participants receive educational materials and personalized counseling based on participant's answers. Participants encouraged to remain active during chemotherapy and/or radiation. Participants receive a booklet that contains a stretching guide with full-body stretches and safety.
Arm Title
Arm B: Multi-Modal Exercise and Nutrition Program (MMENP)
Arm Type
Experimental
Arm Description
After completion of chemotherapy and/or radiation, 3-6 weeks after surgery, then 3-7 months after surgery: Participants complete 4 questionnaires about physical abilities, motivation, and quality of life. Participant's hand grip strength measured. Participants arm strength measured. Participants asked to rise from a chair without using their arms to push off. Participants complete a 6-minute walk test to see how far participant can walk in 6 minutes. Participants complete a nutritional questionnaire and receive nutritional counseling. Participants receive educational materials and personalized counseling based on participant's answers. Participants complete moderate-intensity aerobic exercise 5 days each week. Participants complete strength training exercises 2 times per week. Participants contacted by phone by member of study staff 1 time each week for the first 4 weeks, and then every 2 weeks after that for behavioral skills training and to see how participant is doing.
Intervention Type
Behavioral
Intervention Name(s)
Questionnaires
Other Intervention Name(s)
Surveys
Intervention Description
Participants complete 4 questionnaires about physical abilities, motivation, and quality of life They should take about 25 minutes total to complete.
Intervention Type
Behavioral
Intervention Name(s)
Nutritional Questionnaire and Nutritional Counseling
Intervention Description
Participants complete a nutritional questionnaire and receive nutritional counseling. It should take about 5 minutes to complete. Participants receive educational materials and personalized counseling based on participant's answers.
Intervention Type
Other
Intervention Name(s)
Booklet
Other Intervention Name(s)
Pamphlet, Educational materials
Intervention Description
Participants receive a booklet that contains a stretching guide with full-body stretches and safety.
Intervention Type
Behavioral
Intervention Name(s)
Aerobic Exercise and Strength Training Exercises
Intervention Description
Participants complete up to 30 minutes of moderate-intensity aerobic exercise (such as brisk walking, stationary cycling, and/or elliptical or stair stepping machines) for at least 5 days each week. Participants complete strength training exercises at least 2 times per week.
Intervention Type
Behavioral
Intervention Name(s)
Phone Calls
Intervention Description
Participants contacted by phone by member of study staff one (1) time each week for the first 4 weeks, and then every 2 weeks after that for behavioral skills training and to see how participant is doing. These calls should last about 15 minutes.
Intervention Type
Behavioral
Intervention Name(s)
Physical Assessments
Intervention Description
After completion of chemotherapy and/or radiation, 3-6 weeks after surgery, and then 3-7 months after surgery: Participant's hand grip strength measured using a hand-held machine. Participants arm strength measured using an arm curl test. Participants asked to rise from a chair without using their arms to push off. Participants complete a 6-minute walk test to see how far participant can walk in 6 minutes.
Primary Outcome Measure Information:
Title
Change in 6 Minute Walk Test (6MWT)
Description
Primary endpoint is the change in 6MWT distance, measured in meters, between the time at which preoperative therapy is administered (T0) and the time at which it ends (T1).
Time Frame
Change compared from baseline to date surgery is scheduled

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pancreatic cancer of any type, biopsy-proven Scheduled to receive preoperative therapy (chemotherapy, radiation or chemoradiation) either on- or off-protocol. Anticipated to undergo pancreatectomy in >/= 6 weeks from enrollment Able to understand the description of the study and willing to participate Able to understand the exercise program Able to maintain daily exercise logs Telephone or email access and agreement to engage with the research personnel via phone or email Meet all screening requirements. Exclusion Criteria: Non-English speaking Unable to complete the baseline assessment questionnaires or functional assessments Underlying unstable cardiac or pulmonary disease or symptomatic cardiac disease (New York Heart Association functional class III or IV) Recent fracture or acute musculoskeletal injury that precludes the ability to weight bear fully on all 4 limbs in order to participate in an exercise intervention Numeric pain rating scale of >/= 7 out of 10 Myopathic or rheumatologic disease that impacts physical function Recurrent cancer following prior resection Neuroendocrine cancer Completed preoperative therapy and are on their presurgical rest period.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthew H. Katz, MD
Organizational Affiliation
M.D. Anderson Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas MD Anderson Cancer Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.mdanderson.org
Description
MD Anderson Cancer Center

Learn more about this trial

PancFit: Multimodal Exercise During Preoperative Therapy for Pancreatic Cancer

We'll reach out to this number within 24 hrs