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Prehabilitation During the Neoadjuvant Window of Opportunity in Older Women With Ovarian Cancer (FIT4SURGERY)

Primary Purpose

Ovarian Cancer, Neoadjuvant Chemotherapy, Prehabilitation

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
FIT4SURGERY
Healthy Lifestyle Control
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Ovarian Cancer focused on measuring ovarian cancer, neoadjuvant chemotherapy, chemotherapy, physical activity, prehabilitation

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Female; ≥ 60 years of age
  • Diagnosed with ovarian, fallopian tube or primary peritoneal cancer and undergoing planned neoadjuvant chemotherapy and are expecting to undergo planned surgery
  • Fluent in spoken and written English
  • Own a smartphone
  • Have access to the internet to complete assessments

Exclusion Criteria:

  • Patients receiving planned chemotherapy only
  • Patients with uncontrolled cardiovascular disease, who are non-ambulatory, or who have severe cognitive or functional limitations precluding their ability to participate in a physical activity intervention
  • Pregnant women or prisoners
  • Patients whose oncologist has not provided clearance for their participation

Sites / Locations

  • Northwestern UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

FIT4SURGERY Intervention

Healthy Lifestyle Control

Arm Description

The Fit4Surgery intervention consists of the FitBit Inspire HR device, the Fit4Surgery mobile app, and weekly coaching calls.

The Healthy Lifestyle Control group engages in their usual activities and receives education about physical activity and a healthy lifestyle for ovarian cancer patients. They receive weekly check in calls.

Outcomes

Primary Outcome Measures

Proportion of patients who are evaluable for both baseline and post-intervention assessments
Evaluability will be measured for all patients enrolled in the study regardless of intervention assignment. Patients will be considered evaluable if they complete both the pre-intervention baseline assessments (frailty, PROs) and the post-intervention pre-surgery assessments. The proportion of patients evaluable, according to the above definition, over all patients enrolled will be calculated.
Proportion of patients who are adherent to the Fit4Surgery intervention measured among those in the Fit4Surgery arm.
Adherence will be measured in the Fit4Surgery arm. Patients will be considered adherent to the Fit4Surgery intervention if they wear their Fitbit for >70% of the days during the study period (i.e., ~44/63 days) and if they meet their physical activity goals (step count) on >70% of the days during the study period. The proportion of patients in the Fit4Surgery arm who are adherent to the intervention, according to the above definition, will be calculated.

Secondary Outcome Measures

Change in frailty
Frailty will be assessed at baseline and prior to surgery using the "Fried's phenotype method" in patients in both groups. According to this scale, patients will be categorized as non-frail, pre-frail or frail.
Change in anxiety
Anxiety will be measured using "PROMIS anxiety short form 7a" measure.
Change in physical function
Physical function will be measured using "PROMIS physical function short form 10a" measure.
Change in fatigue
Fatigue will be measured using "PROMIS fatigue short form 7a" measure.
Adverse Events
The number of adverse events will be recorded and graded according to CTCAE v5.0.
Surgical Complications
Medical record review will be performed to examine postoperative complications which will be graded using the Clavien-Dindo scale.
Progression free survival
Medical records will be reviewed for up to three years to monitor for cancer recurrence.
Overall survival
Medical records will be reviewed for up to three years to monitor for overall survival.

Full Information

First Posted
August 13, 2021
Last Updated
January 15, 2023
Sponsor
Northwestern University
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1. Study Identification

Unique Protocol Identification Number
NCT05092763
Brief Title
Prehabilitation During the Neoadjuvant Window of Opportunity in Older Women With Ovarian Cancer
Acronym
FIT4SURGERY
Official Title
A Pilot Study of Prehabilitation During the Neoadjuvant Window of Opportunity in Older Women With Ovarian Cancer (FIT4SURGERY)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 10, 2021 (Actual)
Primary Completion Date
August 2023 (Anticipated)
Study Completion Date
August 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University

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
The purpose of this study is to test the effectiveness of a home-based, patient-tailored intervention, FIT4SURGERY, to promote physical activity among women with ovarian cancer undergoing neoadjuvant chemotherapy.
Detailed Description
Ovarian cancer is the deadliest gynecologic cancer with 5-year survival rates of approximately 48%. Standard of care treatment is grueling, requiring a radical "debulking" surgery and 5 months of chemotherapy. Cytoreductive surgery for ovarian cancer is often extensive, due to the necessary removal of all visible cancer. This radical surgery results in major postoperative complication rates as high as 50% in prospective clinical trials, and 75% occur within 2 weeks of surgery. Half of women are greater than 60 years-old and have high rates of hospital readmission and postoperative complications. Aside from immediate morbidity and mortality related to surgery itself, postoperative complications, such as anastomotic leak, sepsis, or pelvic abscess, can delay the onset of adjuvant chemotherapy, resulting in decreased survival. These postoperative complications also lead to increased discharge to a non-home setting, decreased quality of life, increased costs, and mortality. Although all patients with ovarian cancer undergo this treatment schedule, older women are at particularly high risk for adverse events. Among women with ovarian cancer, more than 50% are over the age of 60 and up to 40% of these older women are defined as frail. Both age and frailty have been shown to be independent predictors of surgical complications, chemotherapy complications, as well as under-treatment with chemotherapy, resulting in inferior cancer-specific survival. Additionally, the definition of aging contains mechanisms beyond the chronological age of the patient. Both a cancer diagnosis and receipt of chemotherapy lead to synergistic biologic and physiologic changes that accelerate aging and increase frailty. Many older women with ovarian cancer are treated with neoadjuvant chemotherapy which is delivered in 3-4 cycles prior to surgery and this time period provides an optimal window to intervene to improve high-risk older patients' surgical outcomes. Prehabilitation is the process of enhancing an individual's functional capacity prior to a forthcoming stressor, such as a major surgery, with the goal of improving postoperative outcomes. Prehabilitation programs are multimodal and can involve medical optimization, preoperative physical exercise, nutritional support and stress/anxiety reduction. Benefits of prehabilitation include reduced length of stay, fewer postoperative complications and improved postoperative pain. Even small increases in light physical activity or reducing sedentary time has been shown to slow or halt functional decline and improve quality of life. Among advanced cancer patients, physical activity interventions have been shown to be safe and feasible. They have also been associated with improved aerobic capacity, increased strength, and increased physical function. These parameters are important in older ovarian cancer patients to prevent functional decline, reduce frailty, and decrease surgical morbidity. However, not all prehabilitation interventions or physical activity interventions are effective. There are populations that do not have sufficient time prior to surgery to have a meaningful change in activity or nutrition, this is especially true for cancer patients who often have a short window between diagnosis and surgery. Furthermore, many physical activity interventions in the pre-operative period have used structured, in-person, professionally-led programs with high intensity activity that may not be appropriate for the changing symptom burden of older ovarian cancer patients undergoing chemotherapy. Instead of a one-size fits all approach, the American Cancer Society recommends that patients with advanced cancer engage in physical activity tailored to their capability. A recent systematic review and meta-analysis of prehabilitation in cancer patients undergoing abdominal operations noted that data specific to older patients are sparse. This study seeks to address this critical research gap by testing a home-based, patient-tailored, physical activity prehabilitation program (FIT4SURGERY) among older women with ovarian cancer undergoing neoadjuvant chemotherapy. Physical activity has been shown to improve functional health and energy balance as well as decrease rates of frailty and sarcopenia, important prognostic factors prior to surgery, especially for older adults, and important prognostic factors for ovarian cancer. Increasing physical activity and motivating behavior change is difficult and many preoperative physical activity interventions have not utilized techniques and frameworks which have been successfully used among patients with chronic diseases. Social cognitive theory (SCT) is a framework which has been successfully used to design physical activity inventions that lead to behavior change. SCT has three main components, self-monitoring, self-judgment and self-evaluation which all contribute to self-regulation which is ultimately what drives behavior change. Behavioral interventions using SCT frameworks have been studied in healthy participants including cancer survivors, and have been shown to increase physical activity. Among women with metastatic breast cancer undergoing chemotherapy, an mHealth behavioral physical activity intervention consisting of a wearable activity tracker to provide direct feedback and a mobile app with motivational messaging, has been implemented by our research group. This study examines a modified version of this intervention, as prehabilitation, for the older ovarian cancer patient, as SCT-driven physical activity interventions have not been studied in a preoperative population. Compared to the gold standard of professionally led, physical activity interventions, interventions via phone and email have been shown to be potentially as effective as more resource intensive interventions at increasing physical activity. Interventions using mHealth app-based platforms have also been shown to increase physical activity. Specifically, for older patients with ovarian cancer undergoing chemotherapy, interventions using wearable devices may be useful because they are home-based, easy to use, give immediate feedback, and use technology most patients already own. Caregivers can also be enlisted to help patients; activating social support for physical activity. Wearable devices allow for remote monitoring of participants and prevent the need for in-person visits which may be difficult for patients undergoing chemotherapy particularly during the COVID-19 pandemic. Furthermore, Fit4Surgery incorporates daily reported symptom burden into activity goals as symptoms can wax and wane during treatment. Such a tailored, home-based, patient-specific approach that facilitates the gradual and safe adoption of physical activity that can be supported by caregivers is ideal for older ovarian cancer patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ovarian Cancer, Neoadjuvant Chemotherapy, Prehabilitation
Keywords
ovarian cancer, neoadjuvant chemotherapy, chemotherapy, physical activity, prehabilitation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
FIT4SURGERY Intervention
Arm Type
Experimental
Arm Description
The Fit4Surgery intervention consists of the FitBit Inspire HR device, the Fit4Surgery mobile app, and weekly coaching calls.
Arm Title
Healthy Lifestyle Control
Arm Type
Active Comparator
Arm Description
The Healthy Lifestyle Control group engages in their usual activities and receives education about physical activity and a healthy lifestyle for ovarian cancer patients. They receive weekly check in calls.
Intervention Type
Behavioral
Intervention Name(s)
FIT4SURGERY
Intervention Description
The Fit4Surgery intervention consists of the FitBit Inspire HR device, the Fit4Surgery mobile app, and weekly coaching calls. Patients are asked to wear the Fitbit through the entire 9-12 weeks in which they are receiving neoadjuvant chemotherapy both when asleep and when awake. Patients are taught how to understand the Fitbit outputs on the application, for example, understanding how to monitor their steps and heart rate. Caregivers are also be encouraged to assist patients. Patients are provided with information about the benefits of physical activity and effective behavior change strategies for incorporating physical activity into their daily lives. These include things such as short bouts of activity by walking around the room during commercial breaks or planning to be dropped off a short walk from a destination.
Intervention Type
Behavioral
Intervention Name(s)
Healthy Lifestyle Control
Intervention Description
Participants assigned to this study arm are instructed to go about their usual activities and receive education about physical activity and a healthy lifestyle for ovarian cancer patients. They are encouraged to download the free Cancer.Net mobile app and visit the cancer.net website for educational materials related to ovarian cancer and survivorship. At the end of the 9-12 week intervention, participants in the Healthy Lifestyle group receive a Fitbit for their optional, personal use after surgery.
Primary Outcome Measure Information:
Title
Proportion of patients who are evaluable for both baseline and post-intervention assessments
Description
Evaluability will be measured for all patients enrolled in the study regardless of intervention assignment. Patients will be considered evaluable if they complete both the pre-intervention baseline assessments (frailty, PROs) and the post-intervention pre-surgery assessments. The proportion of patients evaluable, according to the above definition, over all patients enrolled will be calculated.
Time Frame
Through study completion, average of 9-12 weeks
Title
Proportion of patients who are adherent to the Fit4Surgery intervention measured among those in the Fit4Surgery arm.
Description
Adherence will be measured in the Fit4Surgery arm. Patients will be considered adherent to the Fit4Surgery intervention if they wear their Fitbit for >70% of the days during the study period (i.e., ~44/63 days) and if they meet their physical activity goals (step count) on >70% of the days during the study period. The proportion of patients in the Fit4Surgery arm who are adherent to the intervention, according to the above definition, will be calculated.
Time Frame
Through study completion, average of 9-12 weeks
Secondary Outcome Measure Information:
Title
Change in frailty
Description
Frailty will be assessed at baseline and prior to surgery using the "Fried's phenotype method" in patients in both groups. According to this scale, patients will be categorized as non-frail, pre-frail or frail.
Time Frame
Baseline and once at 9-12 weeks
Title
Change in anxiety
Description
Anxiety will be measured using "PROMIS anxiety short form 7a" measure.
Time Frame
Baseline and once at 9-12 weeks
Title
Change in physical function
Description
Physical function will be measured using "PROMIS physical function short form 10a" measure.
Time Frame
Baseline and once at 9-12 weeks
Title
Change in fatigue
Description
Fatigue will be measured using "PROMIS fatigue short form 7a" measure.
Time Frame
Baseline and once at 9-12 weeks
Title
Adverse Events
Description
The number of adverse events will be recorded and graded according to CTCAE v5.0.
Time Frame
Once at 9-12 weeks
Title
Surgical Complications
Description
Medical record review will be performed to examine postoperative complications which will be graded using the Clavien-Dindo scale.
Time Frame
90 days post surgery
Title
Progression free survival
Description
Medical records will be reviewed for up to three years to monitor for cancer recurrence.
Time Frame
three years post surgery
Title
Overall survival
Description
Medical records will be reviewed for up to three years to monitor for overall survival.
Time Frame
three years post surgery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female; ≥ 60 years of age Diagnosed with ovarian, fallopian tube or primary peritoneal cancer and undergoing planned neoadjuvant chemotherapy and are expecting to undergo planned surgery Fluent in spoken and written English Own a smartphone Have access to the internet to complete assessments Exclusion Criteria: Patients receiving planned chemotherapy only Patients with uncontrolled cardiovascular disease, who are non-ambulatory, or who have severe cognitive or functional limitations precluding their ability to participate in a physical activity intervention Pregnant women or prisoners Patients whose oncologist has not provided clearance for their participation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Emma Barber, MD, MS
Phone
3124724684
Email
emma.barber@northwestern.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Anne Grace, PhD
Phone
3125034165
Email
anne@northwestern.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emma Barber, MD, MS
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne Grace, PhD
Phone
312-503-4165
Email
anne@northwestern.edu
First Name & Middle Initial & Last Name & Degree
Brenda Vega
Email
brenda.vega@northwestern.edu
First Name & Middle Initial & Last Name & Degree
Emma Barber, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Prehabilitation During the Neoadjuvant Window of Opportunity in Older Women With Ovarian Cancer

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