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Trimodal Prehabilitation for Cystectomy Patients to Enhance Post-operative Care (TPC-RCT)

Primary Purpose

Bladder Cancer, Nutrition Aspect of Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Trimodal Prehab & ERP
No Prehab; ERP Alone
Sponsored by
Jason Martyn
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bladder Cancer focused on measuring cystectomy, nutrition, physiotherapy, prehabilitation, enhanced recovery after surgery

Eligibility Criteria

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

Inclusion Criteria:

  1. Male or female ≥ 18 years of age at time of consent for surgery.
  2. Documentation of bladder cancer diagnosis as evidenced by diagnostic imaging and biopsy.
  3. May or may not receive adjuvant therapy.
  4. Written informed consent obtained from subject

Exclusion Criteria:

  1. Presence of a condition or abnormality that in the opinion of the investigator would compromise the safety of the patient or adherence to the program. This includes:

    1. American Society of Anesthesiologists (ASA) health class status 4-5;
    2. Co-morbid medical, physical, and/or mental conditions including dementia, disabling orthopedic and neuromuscular disease, psychosis;
    3. Severe cardiac abnormalities, end-stage organ disease, sepsis, or morbid obesity (BMI greater than 35);
  2. Undergoing radical cystectomy for a reason other than bladder cancer.
  3. Poor comprehension of English or French
  4. Screened by Total Cardiology staff and determined to be inappropriate for prehabilitation at their facility.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Trimodal Prehab & ERP

    No Prehab; ERP Alone

    Arm Description

    Trimodal prehab includes: Guided exercise program at Repsol Place in Calgary, Alberta 2x/week, hosted by the Total Cardiology group. Home-exercise program for another 3x/week. Nutritional optimization with a high-protein oral supplement, along with nutritional counseling and access to a Registered Dietitian on site. Anxiety reduction workshop and take-home anxiety reduction program.

    The active comparator group will be given a home exercise program, nutrition education, and a take-home anxiety reduction program.

    Outcomes

    Primary Outcome Measures

    6-minute walk test (6MWT)
    The 6MWT is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity.

    Secondary Outcome Measures

    10-meter walk test (10mWT)
    The 10 Metre Walk Test is a performance measure used to assess walking speed in metres per second over a short distance. It can be employed to determine functional mobility, gait, and vestibular function.
    30s sit-to-stand test (30CST)
    The 30CST is a measurement that assesses functional lower extremity strength in older adults. It is part of the Fullerton Functional Fitness Test Battery. This test was developed to overcome the floor effect of the 5 or 10 repetition sit to stand test in older adults.
    Hand-grip dynamometry
    A quantitative and objective measure of isometric muscular strength of the hand and forearm, predictive of overall upper-extremity function.
    Functional Assessment of Cancer Therapy for Bladder Cancer (FACT-Bl)Questionnaire
    A reliable and valid questionnaire that comprehensively assesses quality of life concerns pertinent to bladder cancer patients.
    EuroQOL five dimensions (EQ-5D) Questionnaire
    A short, generic quality of life questionnaire
    Godin Leisure Time Exercise Questionnaire
    A short questionnaire on self-reported physical activity.

    Full Information

    First Posted
    November 14, 2017
    Last Updated
    November 16, 2017
    Sponsor
    Jason Martyn
    Collaborators
    Alberta Health services, University of Calgary, Physiotherapy Alberta - College + Association, University of Alberta
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03347045
    Brief Title
    Trimodal Prehabilitation for Cystectomy Patients to Enhance Post-operative Care
    Acronym
    TPC-RCT
    Official Title
    Trimodal Prehabilitation for Cystectomy Patients to Enhance Post-operative Care: A Randomized Control Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2017
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 15, 2018 (Anticipated)
    Primary Completion Date
    January 15, 2019 (Anticipated)
    Study Completion Date
    July 15, 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Jason Martyn
    Collaborators
    Alberta Health services, University of Calgary, Physiotherapy Alberta - College + Association, University of Alberta

    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
    Trimodal prehabilitation is a preoperative three-tiered (trimodal) approach to optimizing physical and mental health. It has been found to successfully improve functional recovery in patients undergoing colorectal surgery following an evidence-based enhanced-recovery pathway (ERP). It is unknown whether the same program is effective in patients undergoing a similar surgery for bladder cancer (radical cystectomy). Objective: To evaluate the appropriateness of a standardized prehabilitation program for implementation into an enhanced recovery pathway for cystectomy patients and determine whether prehabilitation facilitates earlier recovery of functional capacity. Hypothesis: Prehabilitation will ultimately improve recovery of functional capacity, clinical and patient-centered outcomes in patients undergoing radical cystectomy for bladder cancer. Design: Participants will follow an 8-week trimodal prehabilitation program consisting of exercise therapy combined with nutritional counseling, protein supplementation, and psychological care; they will be compared to a cohort of participants following ERP care alone. Conclusion: The proposal will provide insight into the feasibility and effectiveness of trimodal prehabilitation for radical cystectomy patients and may ultimately lead to improved clinical outcomes and reduced morbidity.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Bladder Cancer, Nutrition Aspect of Cancer
    Keywords
    cystectomy, nutrition, physiotherapy, prehabilitation, enhanced recovery after surgery

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Single-center pragmatic randomized-control trial.
    Masking
    Outcomes Assessor
    Masking Description
    Assessor blinding; due to the nature of the study, participant, care provider & investigator cannot be blinded.
    Allocation
    Randomized
    Enrollment
    50 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Trimodal Prehab & ERP
    Arm Type
    Experimental
    Arm Description
    Trimodal prehab includes: Guided exercise program at Repsol Place in Calgary, Alberta 2x/week, hosted by the Total Cardiology group. Home-exercise program for another 3x/week. Nutritional optimization with a high-protein oral supplement, along with nutritional counseling and access to a Registered Dietitian on site. Anxiety reduction workshop and take-home anxiety reduction program.
    Arm Title
    No Prehab; ERP Alone
    Arm Type
    Active Comparator
    Arm Description
    The active comparator group will be given a home exercise program, nutrition education, and a take-home anxiety reduction program.
    Intervention Type
    Combination Product
    Intervention Name(s)
    Trimodal Prehab & ERP
    Other Intervention Name(s)
    Trimodal prehab and enhanced-recovery pathway (ERP) together
    Intervention Description
    1-hr daily exercise will be completed a total of 5d/week, of which 2 of these sessions are completed through a community fitness center. Following these sessions, the participant will consume a high-protein oral supplement. Additionally, during the program, participants will be given the option of attending a stress-reduction group and will receive a take-home anxiety-reduction program. They will have access to a physiotherapist, kinesiologist, registered dietitian, and physician throughout the program. The total length of this program is 8-weeks and is timed to occur in the waiting period between the consent for surgery and operation date.
    Intervention Type
    Other
    Intervention Name(s)
    No Prehab; ERP Alone
    Other Intervention Name(s)
    No trimodal prehab; enhanced-recovery pathway (ERP) alone
    Intervention Description
    1-hr daily exercise with a self-completed home-exercise program. The participant will be given nutritional education material and a take-home anxiety-reduction program. They will be responsible for maintaining a journal of their activity.
    Primary Outcome Measure Information:
    Title
    6-minute walk test (6MWT)
    Description
    The 6MWT is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity.
    Time Frame
    Multiple time-points over 20-weeks
    Secondary Outcome Measure Information:
    Title
    10-meter walk test (10mWT)
    Description
    The 10 Metre Walk Test is a performance measure used to assess walking speed in metres per second over a short distance. It can be employed to determine functional mobility, gait, and vestibular function.
    Time Frame
    Multiple time-points over 20-weeks
    Title
    30s sit-to-stand test (30CST)
    Description
    The 30CST is a measurement that assesses functional lower extremity strength in older adults. It is part of the Fullerton Functional Fitness Test Battery. This test was developed to overcome the floor effect of the 5 or 10 repetition sit to stand test in older adults.
    Time Frame
    Multiple time-points over 20-weeks
    Title
    Hand-grip dynamometry
    Description
    A quantitative and objective measure of isometric muscular strength of the hand and forearm, predictive of overall upper-extremity function.
    Time Frame
    Multiple time-points over 20-weeks
    Title
    Functional Assessment of Cancer Therapy for Bladder Cancer (FACT-Bl)Questionnaire
    Description
    A reliable and valid questionnaire that comprehensively assesses quality of life concerns pertinent to bladder cancer patients.
    Time Frame
    Collected at beginning and end of 20-week participant involvement period
    Title
    EuroQOL five dimensions (EQ-5D) Questionnaire
    Description
    A short, generic quality of life questionnaire
    Time Frame
    Collected at beginning and end of 20-week participant involvement period
    Title
    Godin Leisure Time Exercise Questionnaire
    Description
    A short questionnaire on self-reported physical activity.
    Time Frame
    Collected at beginning and end of 20-week participant involvement period
    Other Pre-specified Outcome Measures:
    Title
    Length of hospital stay (LOS)
    Description
    Length of stay in the hospital starting from post-operative day #0 and terminating when the participant is discharged from the hospital.
    Time Frame
    Collected at the finale of participant-involvement (20-weeks)
    Title
    30 day readmission rate
    Description
    Number of participants re-admitted to hospital within 30 days of discharge as a percentage of the total number of participants involved in the study.
    Time Frame
    Collected at the finale of participant-involvement (20-weeks)
    Title
    Clavien-Dindo classification of Surgical Complications
    Description
    A classification scheme that objectively grades surgical complications using a descriptive grading system.
    Time Frame
    Collected at the finale of participant-involvement (20-weeks)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Male or female ≥ 18 years of age at time of consent for surgery. Documentation of bladder cancer diagnosis as evidenced by diagnostic imaging and biopsy. May or may not receive adjuvant therapy. Written informed consent obtained from subject Exclusion Criteria: Presence of a condition or abnormality that in the opinion of the investigator would compromise the safety of the patient or adherence to the program. This includes: American Society of Anesthesiologists (ASA) health class status 4-5; Co-morbid medical, physical, and/or mental conditions including dementia, disabling orthopedic and neuromuscular disease, psychosis; Severe cardiac abnormalities, end-stage organ disease, sepsis, or morbid obesity (BMI greater than 35); Undergoing radical cystectomy for a reason other than bladder cancer. Poor comprehension of English or French Screened by Total Cardiology staff and determined to be inappropriate for prehabilitation at their facility.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Jason Martyn, MScPT
    Phone
    403-943-3575
    Email
    jason.martyn@ahs.ca
    First Name & Middle Initial & Last Name or Official Title & Degree
    Chelsia Gillis, PhD
    Email
    chelsia.gillis@ucalgary.ca
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jason Martyn, MScPT
    Organizational Affiliation
    Alberta Health services
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Trimodal Prehabilitation for Cystectomy Patients to Enhance Post-operative Care

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