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Effect of Prehabilitation on Surgical Outcomes of Abdominally-based Plastic Surgery Procedures

Primary Purpose

Ventral Hernia, Panniculus, Abdominoplasty

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Prehabilitation Program
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ventral Hernia

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

- Adult patients (>18 years) who are undergoing elective abdominally-based plastic surgery operations in 3+ weeks by one of the following plastic surgeons: Nazerali, Lee, Murphy, Nguyen, Lorenz.

Exclusion Criteria:

  • Patients who do not speak English
  • Patients who do not have access to a smartphone or internet/cell service.
  • Patients who are undergoing another intervention study that consists of a nutrition and/or exercise behavior change.

Sites / Locations

  • Stanford Cancer Center South BayRecruiting
  • Stanford Plastic and Reconstructive Surgery ClinicRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Prehab Intervention Arm

Arm Description

The control arm will receive no additional prehabilitation material prior to material. Rather, they will receive standard preoperative care in which they will be given standard advice on nutrition and fitness. REDcap surveys will be administered.

The intervention arm will receive access to the prehab program (abdominal workout videos) and surveys via RedCAP.The program will start no less than 14 days before the date of surgery.

Outcomes

Primary Outcome Measures

Occurrence of surgical complications (Post-op days 7-14)
Will analyze the occurrence of surgical complications after surgery. Hematoma, seroma, or abscess.
Occurrence of surgical complications (Post-op day 30)
Will analyze the occurrence of surgical complications after surgery. Hematoma, seroma, or abscess.
Occurrence of surgical complications (Post-op day 90)
Will analyze the occurrence of surgical complications after surgery. Hematoma, seroma, or abscess.
Occurrence of surgical complications (Post-op day 180)
Will analyze the occurrence of surgical complications after surgery. Hematoma, seroma, or abscess.
Occurrence of surgical complications (Post-op day 360)
Will analyze the occurrence of surgical complications after surgery. Hematoma, seroma, or abscess.
Patient-Reported Outcome Measures: RAND 36-Item Health Survey (RAND-36) on Post-op days 7-14
Will use the RAND 36-Item Health Survey (RAND-36) to assess the patient's perceived health following their surgical procedure. The score for RAND-36 ranges from 0-100, having higher scores mean better outcomes.
Patient-Reported Outcome Measures: Abdominal Surgery Impact Scale (ASIS) on Post-op days 7-14
Will use the Abdominal Surgery Impact Scale (ASIS) to assess the patient's perceived health following their surgical procedure. The ASIS score ranges from 18-126, having higher scores indicate better quality of life.
Patient-Reported Outcome Measures: RAND 36-Item Health Survey (RAND-36) on Post-op day 30
Will use the RAND 36-Item Health Survey (RAND-36) to assess the patient's perceived health following their surgical procedure. The score for RAND-36 ranges from 0-100, having higher scores mean better outcomes.
Patient-Reported Outcome Measures: Abdominal Surgery Impact Scale (ASIS) on Post-op day 30
Will use the Abdominal Surgery Impact Scale (ASIS) to assess the patient's perceived health following their surgical procedure. The ASIS score ranges from 18-126, having higher scores indicate better quality of life.
Patient-Reported Outcome Measures: RAND 36-Item Health Survey (RAND-36) on Post-op day 90
Will use the RAND 36-Item Health Survey (RAND-36) to assess the patient's perceived health following their surgical procedure. The score for RAND-36 ranges from 0-100, having higher scores mean better outcomes.
Patient-Reported Outcome Measures: Abdominal Surgery Impact Scale (ASIS) on Post-op day 90
Will use the Abdominal Surgery Impact Scale (ASIS) to assess the patient's perceived health following their surgical procedure. The ASIS score ranges from 18-126, having higher scores indicate better quality of life.
Patient-Reported Outcome Measures: RAND 36-Item Health Survey (RAND-36) on Post-op day 180
Will use the RAND 36-Item Health Survey (RAND-36) to assess the patient's perceived health following their surgical procedure. The score for RAND-36 ranges from 0-100, having higher scores mean better outcomes.
Patient-Reported Outcome Measures: Abdominal Surgery Impact Scale (ASIS) on Post-op day 180
Will use the Abdominal Surgery Impact Scale (ASIS) to assess the patient's perceived health following their surgical procedure. The ASIS score ranges from 18-126, having higher scores indicate better quality of life.
Patient-Reported Outcome Measures: RAND 36-Item Health Survey (RAND-36) on Post-op day 360
Will use the RAND 36-Item Health Survey (RAND-36) to assess the patient's perceived health following their surgical procedure. The score for RAND-36 ranges from 0-100, having higher scores mean better outcomes.
Patient-Reported Outcome Measures: Abdominal Surgery Impact Scale (ASIS) on Post-op day 360
Will use the Abdominal Surgery Impact Scale (ASIS) to assess the patient's perceived health following their surgical procedure. The ASIS score ranges from 18-126, having higher scores indicate better quality of life.
Physical Function Test: 6-minute walk test at Time of Enrollment
Will use the 6-minute walk test. The 6-minute walk test will be used to assess aerobic capacity and endurance. A normal walk distance ranges from 400 to 700 m.
Physical Function Test: 5-times-sit-to-stand test at Time of Enrollment
Will use the 5-times-sit-to-stand test. The 5-times-sit-to-stand test is a method to quantify functional lower extremity strength. Lower times indicate better scores.
Physical Function Test: Timed-up-and-go test at Time of Enrollment
Will use the timed-up-and-go test. The timed-up-and go test assesses one's mobility. A lower score signifies better mobility.
Physical Function Test: 6-minute walk test at 3 weeks
Will use the 6-minute walk test. The 6-minute walk test will be used to assess aerobic capacity and endurance. A normal walk distance ranges from 400 to 700 m.
Physical Function Test: 5-times-sit-to-stand test at 3 weeks
Will use the 5-times-sit-to-stand test. The 5-times-sit-to-stand test is a method to quantify functional lower extremity strength. Lower times indicate better scores.
Physical Function Test: Timed-up-and-go test at 3 weeks
Will use the timed-up-and-go test. The timed-up-and go test assesses one's mobility. A lower score signifies better mobility.
Physical Function Test: 6-minute walk test on Post-op Day 30
Will use the 6-minute walk test. The 6-minute walk test will be used to assess aerobic capacity and endurance. A normal walk distance ranges from 400 to 700 m.
Physical Function Test: 5-times-sit-to-stand-test on Post-op Day 30
Will use the 5-times-sit-to-stand test. The 5-times-sit-to-stand test is a method to quantify functional lower extremity strength. Lower times indicate better scores.
Physical Function Test: Timed-up-and-go test on Post-op Day 30
Will use the timed-up-and-go test. The timed-up-and go test assesses one's mobility. A lower score signifies better mobility.
Physical Function Test: 6-minute walk test on Post-op Day 90
Will use the 6-minute walk test. The 6-minute walk test will be used to assess aerobic capacity and endurance. A normal walk distance ranges from 400 to 700 m.
Physical Function Test: 5-times-sit-to-stand test on Post-op Day 90
Will use the 5-times-sit-to-stand test. The 5-times-sit-to-stand test is a method to quantify functional lower extremity strength. Lower times indicate better scores.
Physical Function Test: Timed-up-and-go test on Post-op Day 90
Will use the timed-up-and-go test. The timed-up-and go test assesses one's mobility. A lower score signifies better mobility.

Secondary Outcome Measures

Change from Baseline Albumin Levels at Time of Surgery
To analyze nutritional status
Change from Baseline Prealbumin Levels at Time of Surgery
To analyze nutritional status
Change from Baseline Transferrin Levels at Time of Surgery
To analyze nutritional status
Change from Baseline C-reactive Protein Levels at Time of Surgery
To analyze level of physiologic inflammation
Change from Baseline Erythrocyte Sedimentation Rates at Time of Surgery
To analyze level of physiologic inflammation
Change from Baseline Hemoglobin A1C Levels at Time of Surgery
To analyze degree of diabetes mellitus control
Change from Baseline Plasma Glucose Levels at Time of Surgery
To analyze degree of diabetes mellitus control
Change from Baseline White Blood Cell Count at Time of Surgery
Assessment for leukocytosis, anemia, renal disease; Part of the complete blood count.
Change from Baseline Hemoglobin Levels at Time of Surgery
Assessment for leukocytosis, anemia, renal disease; Part of the complete blood count.
Change from Baseline Hematocrit Levels at Time of Surgery
Assessment for leukocytosis, anemia, renal disease; Part of the complete blood count.
Change from Baseline Platelet Levels at Time of Surgery
Assessment for leukocytosis, anemia, renal disease; Part of the complete blood count.
Change from Baseline Chloride Levels at Time of Surgery
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Change from Baseline Sodium Levels at Time of Surgery
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Change from Baseline Potassium Levels at Time of Surgery
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Change from Baseline Carbon Dioxide Levels at Time of Surgery
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Change from Baseline Blood Urea Nitrogen Levels at Time of Surgery
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Change from Baseline Creatinine Levels at Time of Surgery
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Change from Baseline Blood Glucose Levels at Time of Surgery
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel

Full Information

First Posted
March 1, 2021
Last Updated
December 14, 2021
Sponsor
Stanford University
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1. Study Identification

Unique Protocol Identification Number
NCT04787874
Brief Title
Effect of Prehabilitation on Surgical Outcomes of Abdominally-based Plastic Surgery Procedures
Official Title
Effect of Health Habits on Outcomes in Plastic and Reconstructive Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Recruiting
Study Start Date
June 21, 2021 (Actual)
Primary Completion Date
May 23, 2025 (Anticipated)
Study Completion Date
June 2, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford 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 determine whether a program to optimize patient physical fitness and nutrition ("prehabilitation") prior to and after plastic surgery involving the abdomen improves surgical outcomes. The investigators hope to determine how a multimodal peri-operative prehabilitation program can be most effective in engaging and motivating patients to physically and mentally get ready for an abdominally-based plastic surgery operation. The overall goal is to determine if this program will improve post-operative recovery after abdominally-based plastic surgery. The importance of this new knowledge is better understanding of ways that plastic surgeons can improve outcomes, engagement, and experience of patients undergoing abdominally-based plastic surgery operations. This would translate to increased healthcare value and better long-term outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ventral Hernia, Panniculus, Abdominoplasty, Flap Reconstruction

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
520 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
The control arm will receive no additional prehabilitation material prior to material. Rather, they will receive standard preoperative care in which they will be given standard advice on nutrition and fitness. REDcap surveys will be administered.
Arm Title
Prehab Intervention Arm
Arm Type
Experimental
Arm Description
The intervention arm will receive access to the prehab program (abdominal workout videos) and surveys via RedCAP.The program will start no less than 14 days before the date of surgery.
Intervention Type
Behavioral
Intervention Name(s)
Prehabilitation Program
Intervention Description
Nutrition component: Participants will receive information on how to follow a healthy diet (Mediterranean-style diet) with emphasis on whole foods, plants, lean protein, olive oil; restriction of red meats, processed meats, processed foods, added sugar) Exercise component: Participants will receive an activity tracker to use during the study period (3+ weeks before surgery, and 30 days after surgery). Participants will be assigned strength exercises to work on core strength and proximal muscle strength (biceps/triceps, quads, hamstrings, calves).The exercises will mainly be focused on strengthening the abdominal wall. Exercises will be tailored to patients' individual capabilities. They will also be assigned cardio exercises - either low-intensity steady state cardio vs High Intensity Interval training. Level of cardio exercise will be tailored based on patient's Duke Activity score and baseline activity.
Primary Outcome Measure Information:
Title
Occurrence of surgical complications (Post-op days 7-14)
Description
Will analyze the occurrence of surgical complications after surgery. Hematoma, seroma, or abscess.
Time Frame
Post-operative days 7-14
Title
Occurrence of surgical complications (Post-op day 30)
Description
Will analyze the occurrence of surgical complications after surgery. Hematoma, seroma, or abscess.
Time Frame
Post-operative day 30
Title
Occurrence of surgical complications (Post-op day 90)
Description
Will analyze the occurrence of surgical complications after surgery. Hematoma, seroma, or abscess.
Time Frame
Post-operative day 90
Title
Occurrence of surgical complications (Post-op day 180)
Description
Will analyze the occurrence of surgical complications after surgery. Hematoma, seroma, or abscess.
Time Frame
Post-operative day 180
Title
Occurrence of surgical complications (Post-op day 360)
Description
Will analyze the occurrence of surgical complications after surgery. Hematoma, seroma, or abscess.
Time Frame
Post-operative day 360
Title
Patient-Reported Outcome Measures: RAND 36-Item Health Survey (RAND-36) on Post-op days 7-14
Description
Will use the RAND 36-Item Health Survey (RAND-36) to assess the patient's perceived health following their surgical procedure. The score for RAND-36 ranges from 0-100, having higher scores mean better outcomes.
Time Frame
Post-operative days 7-14
Title
Patient-Reported Outcome Measures: Abdominal Surgery Impact Scale (ASIS) on Post-op days 7-14
Description
Will use the Abdominal Surgery Impact Scale (ASIS) to assess the patient's perceived health following their surgical procedure. The ASIS score ranges from 18-126, having higher scores indicate better quality of life.
Time Frame
Post-operative days 7-14
Title
Patient-Reported Outcome Measures: RAND 36-Item Health Survey (RAND-36) on Post-op day 30
Description
Will use the RAND 36-Item Health Survey (RAND-36) to assess the patient's perceived health following their surgical procedure. The score for RAND-36 ranges from 0-100, having higher scores mean better outcomes.
Time Frame
Post-operative day 30
Title
Patient-Reported Outcome Measures: Abdominal Surgery Impact Scale (ASIS) on Post-op day 30
Description
Will use the Abdominal Surgery Impact Scale (ASIS) to assess the patient's perceived health following their surgical procedure. The ASIS score ranges from 18-126, having higher scores indicate better quality of life.
Time Frame
Post-operative day 30
Title
Patient-Reported Outcome Measures: RAND 36-Item Health Survey (RAND-36) on Post-op day 90
Description
Will use the RAND 36-Item Health Survey (RAND-36) to assess the patient's perceived health following their surgical procedure. The score for RAND-36 ranges from 0-100, having higher scores mean better outcomes.
Time Frame
Post-operative day 90
Title
Patient-Reported Outcome Measures: Abdominal Surgery Impact Scale (ASIS) on Post-op day 90
Description
Will use the Abdominal Surgery Impact Scale (ASIS) to assess the patient's perceived health following their surgical procedure. The ASIS score ranges from 18-126, having higher scores indicate better quality of life.
Time Frame
Post-operative day 90
Title
Patient-Reported Outcome Measures: RAND 36-Item Health Survey (RAND-36) on Post-op day 180
Description
Will use the RAND 36-Item Health Survey (RAND-36) to assess the patient's perceived health following their surgical procedure. The score for RAND-36 ranges from 0-100, having higher scores mean better outcomes.
Time Frame
Post-operative day 180
Title
Patient-Reported Outcome Measures: Abdominal Surgery Impact Scale (ASIS) on Post-op day 180
Description
Will use the Abdominal Surgery Impact Scale (ASIS) to assess the patient's perceived health following their surgical procedure. The ASIS score ranges from 18-126, having higher scores indicate better quality of life.
Time Frame
Post-operative day 180
Title
Patient-Reported Outcome Measures: RAND 36-Item Health Survey (RAND-36) on Post-op day 360
Description
Will use the RAND 36-Item Health Survey (RAND-36) to assess the patient's perceived health following their surgical procedure. The score for RAND-36 ranges from 0-100, having higher scores mean better outcomes.
Time Frame
Post-operative day 360
Title
Patient-Reported Outcome Measures: Abdominal Surgery Impact Scale (ASIS) on Post-op day 360
Description
Will use the Abdominal Surgery Impact Scale (ASIS) to assess the patient's perceived health following their surgical procedure. The ASIS score ranges from 18-126, having higher scores indicate better quality of life.
Time Frame
Post-operative day 360
Title
Physical Function Test: 6-minute walk test at Time of Enrollment
Description
Will use the 6-minute walk test. The 6-minute walk test will be used to assess aerobic capacity and endurance. A normal walk distance ranges from 400 to 700 m.
Time Frame
Time of enrollment
Title
Physical Function Test: 5-times-sit-to-stand test at Time of Enrollment
Description
Will use the 5-times-sit-to-stand test. The 5-times-sit-to-stand test is a method to quantify functional lower extremity strength. Lower times indicate better scores.
Time Frame
Time of enrollment
Title
Physical Function Test: Timed-up-and-go test at Time of Enrollment
Description
Will use the timed-up-and-go test. The timed-up-and go test assesses one's mobility. A lower score signifies better mobility.
Time Frame
Time of enrollment
Title
Physical Function Test: 6-minute walk test at 3 weeks
Description
Will use the 6-minute walk test. The 6-minute walk test will be used to assess aerobic capacity and endurance. A normal walk distance ranges from 400 to 700 m.
Time Frame
3 weeks
Title
Physical Function Test: 5-times-sit-to-stand test at 3 weeks
Description
Will use the 5-times-sit-to-stand test. The 5-times-sit-to-stand test is a method to quantify functional lower extremity strength. Lower times indicate better scores.
Time Frame
3 weeks
Title
Physical Function Test: Timed-up-and-go test at 3 weeks
Description
Will use the timed-up-and-go test. The timed-up-and go test assesses one's mobility. A lower score signifies better mobility.
Time Frame
3 weeks
Title
Physical Function Test: 6-minute walk test on Post-op Day 30
Description
Will use the 6-minute walk test. The 6-minute walk test will be used to assess aerobic capacity and endurance. A normal walk distance ranges from 400 to 700 m.
Time Frame
Post-operative day 30
Title
Physical Function Test: 5-times-sit-to-stand-test on Post-op Day 30
Description
Will use the 5-times-sit-to-stand test. The 5-times-sit-to-stand test is a method to quantify functional lower extremity strength. Lower times indicate better scores.
Time Frame
Post-operative day 30
Title
Physical Function Test: Timed-up-and-go test on Post-op Day 30
Description
Will use the timed-up-and-go test. The timed-up-and go test assesses one's mobility. A lower score signifies better mobility.
Time Frame
Post-operative day 30
Title
Physical Function Test: 6-minute walk test on Post-op Day 90
Description
Will use the 6-minute walk test. The 6-minute walk test will be used to assess aerobic capacity and endurance. A normal walk distance ranges from 400 to 700 m.
Time Frame
Post-operative day 90
Title
Physical Function Test: 5-times-sit-to-stand test on Post-op Day 90
Description
Will use the 5-times-sit-to-stand test. The 5-times-sit-to-stand test is a method to quantify functional lower extremity strength. Lower times indicate better scores.
Time Frame
Post-operative day 90
Title
Physical Function Test: Timed-up-and-go test on Post-op Day 90
Description
Will use the timed-up-and-go test. The timed-up-and go test assesses one's mobility. A lower score signifies better mobility.
Time Frame
Post-operative day 90
Secondary Outcome Measure Information:
Title
Change from Baseline Albumin Levels at Time of Surgery
Description
To analyze nutritional status
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Prealbumin Levels at Time of Surgery
Description
To analyze nutritional status
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Transferrin Levels at Time of Surgery
Description
To analyze nutritional status
Time Frame
Enrollment to time of surgery
Title
Change from Baseline C-reactive Protein Levels at Time of Surgery
Description
To analyze level of physiologic inflammation
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Erythrocyte Sedimentation Rates at Time of Surgery
Description
To analyze level of physiologic inflammation
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Hemoglobin A1C Levels at Time of Surgery
Description
To analyze degree of diabetes mellitus control
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Plasma Glucose Levels at Time of Surgery
Description
To analyze degree of diabetes mellitus control
Time Frame
Enrollment to time of surgery
Title
Change from Baseline White Blood Cell Count at Time of Surgery
Description
Assessment for leukocytosis, anemia, renal disease; Part of the complete blood count.
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Hemoglobin Levels at Time of Surgery
Description
Assessment for leukocytosis, anemia, renal disease; Part of the complete blood count.
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Hematocrit Levels at Time of Surgery
Description
Assessment for leukocytosis, anemia, renal disease; Part of the complete blood count.
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Platelet Levels at Time of Surgery
Description
Assessment for leukocytosis, anemia, renal disease; Part of the complete blood count.
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Chloride Levels at Time of Surgery
Description
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Sodium Levels at Time of Surgery
Description
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Potassium Levels at Time of Surgery
Description
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Carbon Dioxide Levels at Time of Surgery
Description
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Blood Urea Nitrogen Levels at Time of Surgery
Description
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Creatinine Levels at Time of Surgery
Description
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Time Frame
Enrollment to time of surgery
Title
Change from Baseline Blood Glucose Levels at Time of Surgery
Description
Assessment for leukocytosis, anemia, renal disease; Part of Basic Metabolic Panel
Time Frame
Enrollment to time of surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: - Adult patients (>18 years) who are undergoing elective abdominally-based plastic surgery operations in 3+ weeks by one of the following plastic surgeons: Nazerali, Lee, Murphy, Nguyen, Lorenz. Exclusion Criteria: Patients who do not speak English Patients who do not have access to a smartphone or internet/cell service. Patients who are undergoing another intervention study that consists of a nutrition and/or exercise behavior change.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cara Black, PGY-2
Phone
650-723-7001
Email
carablack@stanford.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cindy Kin, MD
Organizational Affiliation
Asst Prof-Med Ctr Line
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Cara Black, MD
Organizational Affiliation
Resident
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford Cancer Center South Bay
City
San Jose
State/Province
California
ZIP/Postal Code
95124
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rahim Nazerali, MD, MHS
Facility Name
Stanford Plastic and Reconstructive Surgery Clinic
City
Stanford
State/Province
California
ZIP/Postal Code
94304
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rahim Nazerali, MD, MHS

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Effect of Prehabilitation on Surgical Outcomes of Abdominally-based Plastic Surgery Procedures

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