PACE: Diet and Exercise After Pancreatic Cancer
Study Details
Study Description
Brief Summary
Determine feasibility of a randomized controlled trial (RCT) in pancreatic (& other foregut) cancer patients comparing the effects of diet alone vs. diet+exercise on functional and clinical outcomes.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Foregut cancers such as pancreatic cancer cause significant side effects and poorer health-related quality of life (QOL), as well as a 5-year survival rate of only 6%. Importantly, the reduction in physical functioning caused by this cancer and its therapies is associated with higher mortality risk. Although multiple studies in more prevalent cancer types support exercise benefits (e.g., improved physical functioning), data cannot be generalized from one cancer type to another. Little is known about exercise feasibility and benefits in pancreatic (& other foregut) cancer patients, and no data regarding potential mechanistic outcomes that may explain the link between poor physical performance status and cancer survival have been reported. We will enroll 20 patients with pancreatic adenocarcinoma (or other foregut cancer) who are expected to undergo surgical resection or who are within 3 years of surgical resection, in a pilot project involving a 6-month home-based lifestyle intervention (diet along versus diet+exercise). Research assessments will be done pre-surgery (if applicable), post-surgery (and prior to starting the intervention), 3 months, and 6 months post-surgery. Intervention counseling will be delivered using visual communication (e.g., Skype). Participants will be provided a computer tablet for the intervention with participants randomized to receive exercise counseling also receiving a fitness bracelet to facilitate counseling by the certified Cancer Exercise Trainer. Our primary study aim is to determine feasibility of a randomized controlled trial (RCT) in pancreatic cancer patients comparing the effects of diet alone with diet+exercise on pancreatic cancer-related functional and disease outcomes; feasibility measures include recruitment, retention, intervention adherence, assessment completion, adverse events, and participant satisfaction. Our secondary study aim is to determine the effect of diet+exercise compared with diet alone on physical functioning and QOL. Also, we will draw and store blood samples so that additional funds can be requested to test intervention effects on biomarkers of cancer risk (e.g., tumor immunity, inflammatory cytokines, etc.). The goal of the study is to advance the exercise oncology field into an understudied cancer type and develop an intervention that will improve the survivorship care of pancreatic cancer patients through distance-delivered counseling methods.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Diet only Diet counseling will be delivered using visual communication (e.g., Skype). Participants will be provided a computer tablet for the intervention with participants randomized to receive diet counseling. |
Behavioral: Diet Only
Diet counseling will be delivered using visual communication (e.g., Skype). Participants will be provided a computer tablet for the intervention with participants randomized to receive diet counseling.
|
| Experimental: Diet + Exercise Diet and exercise counseling will be delivered using visual communication (e.g., Skype). Participants will be provided a computer tablet for the intervention with participants randomized to receive diet and exercise counseling also receiving a fitness bracelet to facilitate counseling by the certified Cancer Exercise Trainer. |
Behavioral: Diet + Exercise
Diet and exercise counseling will be delivered using visual communication (e.g., Skype). Participants will be provided a computer tablet for the intervention with participants randomized to receive diet and exercise counseling.
|
Outcome Measures
Primary Outcome Measures
- Feasibility - Recruitment [Baseline]
Number of participants excluded or not agreeing to participate
- Feasibility - Adherence to study protocol activities [Throughout 6 month study period]
Feasibility measure (e.g. percent of assessments completed, percent of counseling sessions completed, etc.)
- Feasibility - Attrition rates [Throughout 6 month study period]
Number of participants who dropout or are withdrawn
- Feasibility - Adverse events [Throughout 6 month study period]
Recorded by staff
- Feasibility - Participant satisfaction [At conclusion of 6 month study period]
Survey
Secondary Outcome Measures
- Eastern Cooperative Oncology Group (ECOG) performance status [At 4 timepoints during the 6 month study (pre-surgery if applicable, post-surgery/prior to starting the intervention, 3 months and 6 months)]
Preliminary effect size
- Quality of life (assessed using the Functional Assessment of Cancer Therapy index) [At 4 timepoints during the 6 month study (pre-surgery if applicable, post-surgery/prior to starting the intervention, 3 months and 6 months)]
Preliminary effect size
- Objective physical functioning [At 4 timepoints during the 6 month study (pre-surgery if applicable, post-surgery/prior to starting the intervention, 3 months and 6 months)]
Preliminary effect size
- CA 19-9 (tumor markers) [At 4 timepoints during the 6 month study (pre-surgery if applicable, post-surgery/prior to starting the intervention, 3 months and 6 months)]
Exploratory data related to within and between group (diet and diet+exercise) differences
- Completion of pancreatic cancer treatment [At conclusion of 6 month study]
Exploratory data related to within and between group (diet and diet+exercise) differences
- Survival rates [At conclusion of 6 month study]
Exploratory data related to within and between group (diet and diet+exercise) differences
- Pancreatic cancer recurrence rates [At conclusion of 6 month study]
Exploratory data related to within and between group (diet and diet+exercise) differences
- Prognostic blood cytokine biomarkers [At 4 timepoints during the 6 month study (pre-surgery if applicable, post-surgery/prior to starting the intervention, 3 months and 6 months)]
Exploratory data related to within and between group (diet and diet+exercise) differences
- Prognostic blood tumor immunity biomarkers [At 4 timepoints during the 6 month study (pre-surgery if applicable, post-surgery/prior to starting the intervention, 3 months and 6 months)]
Exploratory data related to within and between group (diet and diet+exercise) differences
- Wearable activity monitor (weekly minutes of physical activity) [At 4 timepoints during the 6 month study (pre-surgery if applicable, post-surgery/prior to starting the intervention, 3 months and 6 months)]
Exploratory data related to within and between group (diet and diet+exercise) differences
Eligibility Criteria
Criteria
Inclusion Criteria:
-
adult 18 years of age or older with resectable foregut cancer for whom surgery is planned (includes "borderline resectable" if deemed appropriate by surgical investigators) or has occurred within the past 3 years
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English speaking
-
Eastern Cooperative Technology Group (ECOG) performance status of 0,1 or 2.
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able to ambulate without assistance
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able to obtain medical clearance
Exclusion Criteria:
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foregut cancer recurrence
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dementia or organic brain syndrome
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severe emotional distress
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medical, psychological or social characteristic that would interfere with the ability to fully participate in program activities and assessments
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another diagnosis of cancer in the past 5 years (not including skin or cervical cancer in situ).
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oncologist refuses to allow screening for possible study participation
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current participation in another exercise trial
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Alabama at Birmingham | Birmingham | Alabama | United States | 35294 |
Sponsors and Collaborators
- University of Alabama at Birmingham
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- F141218007