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Pilot Study of a Geriatric Intervention After Colorectal and Lung Cancer Surgery

Primary Purpose

Colorectal Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
McCorkle Model Intervention
Sponsored by
H. Lee Moffitt Cancer Center and Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Colorectal Cancer focused on measuring Colon, Geriatric, McCorkle Model, Questionnaire

Eligibility Criteria

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

Inclusion Criteria:

  • Colorectal cancer, stage III or IV, confirmed by histology
  • Abdominal surgery by a University of South Florida (USF) surgeon at Moffitt Cancer Center or Tampa General Hospital (TGH)
  • Age 60 years and older
  • Informed consent
  • Living within a one (1) hour radius of Moffitt

Exclusion Criteria:

  • Discharge planned to a rehabilitation facility or a nursing home
  • Unable to answer the questionnaires (e.g. because of cognitive impairment, blindness, deafness)
  • Post-operative inpatient stay >one (1) month

Sites / Locations

  • H. Lee Moffitt Cancer Center and Research Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control Arm

Intervention arm

Arm Description

Usual post-surgical care

In addition to usual post-surgical care, the patients will receive a 4 week geriatric nurse practitioner-centered intervention, based on the McCorkle model.

Outcomes

Primary Outcome Measures

Feasibility of the Intervention
The primary end-point for the pilot will be the feasibility of the intervention, measured as follows: A compliance of >=90% with the intervention table on page 17 A success rate (improvement or resolution of problems) of >= 80% A completion rate of >=90% of the initial and final study questionnaires

Secondary Outcome Measures

Whether the Intervention is Faithful to Dr. McCorkle's Original Intervention
Aim 2 will be judged qualitatively. Dr. Ruth McCorkle and Dr. Janine Overcash will judge whether the intervention is faithful enough to Dr McCorkle's original intervention and whether it can be carried effectively by the trained personnel.
A Successful Collection and Testing of >=90% of the Samples Tested
Aim 3 will be judged by assessing the percentage of tests that could or not be performed on the Moffitt patients.
Effect Size Estimates for Within-group Changes Between Baseline and 1-month
Aim 4 will be assessed by the activities of daily living (ADL), instrumental activities of daily living (IADL), complications and FACT-colorectal (FACT-C) v.4 questionnaires at baseline and end of intervention.

Full Information

First Posted
August 11, 2011
Last Updated
November 26, 2013
Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Collaborators
Tampa General Hospital, University of South Florida, Yale University
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1. Study Identification

Unique Protocol Identification Number
NCT01416168
Brief Title
Pilot Study of a Geriatric Intervention After Colorectal and Lung Cancer Surgery
Official Title
Pilot Study of a Geriatric Intervention After Colorectal and Lung Cancer Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Completed
Study Start Date
December 2008 (undefined)
Primary Completion Date
April 2013 (Actual)
Study Completion Date
November 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Collaborators
Tampa General Hospital, University of South Florida, Yale University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Surgery for colorectal cancer is a major surgery. People above the age of 60 tend to have a higher risk of complications. Some studies indicate that senior cancer patients might benefit from a home support after surgery by a geriatric nurse practitioner and a team, beside their usual post-operative care. The investigators team is planning a large study to assess whether this approach could help patients with colorectal cancer recover better from their surgery, get better cancer treatment after that (e.g. chemotherapy), and possibly live longer. This study you are asked to take part in is a pilot for this large study.
Detailed Description
Our key background data come from the randomized study conducted by McCorkle et al. After evaluation testing, patients will be randomly assigned (similarly to a coin toss) to one of two possible follow-up groups. One would be a regular post-surgery care group (control group), the other will have in addition a support by geriatric nurse practitioner (intervention group). Patients who are assigned to the intervention group: once they arrive home, in addition to their normal post-surgery care, will receive a once a week home visit by a geriatric nurse practitioner (GNP). The GNP will also call the patient once a week in between. The GNP will check any problem patients may have during their recovery and provide or organize care for it. The GNP has a checklist of problems to address so that we can reliably reproduce our intervention in other patients. The GNP will work together with the patient's various doctors and caregivers, as well as a geriatric team. Some of the visits or the telephone calls maybe tape-recorded so that the research team can evaluate the information provided to the patient. We will record any complication patients might have from surgery. No matter which treatment group the patient is assigned to, at the end of a 4 weeks period, we will repeat the tests we did at the beginning to see how they change.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Colon, Geriatric, McCorkle Model, Questionnaire

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Control Arm
Arm Type
No Intervention
Arm Description
Usual post-surgical care
Arm Title
Intervention arm
Arm Type
Experimental
Arm Description
In addition to usual post-surgical care, the patients will receive a 4 week geriatric nurse practitioner-centered intervention, based on the McCorkle model.
Intervention Type
Other
Intervention Name(s)
McCorkle Model Intervention
Intervention Description
The intervention will consist each week in a home visit and a phone call. The GNP conducting the home visit will identify current problems using a comprehensive geriatric assessment (CGA) and record problems on the Intervention and Recommendation Data Sheet. In addition, the cases will be reviewed at a weekly Intervention Team meeting between the intervention GNP (VM, CV), the geriatrician (VP), and the intervention PI (JO). That team meeting will also record how intervention goals for the various problems are met, using the instruments and criteria developed during our pilot study5. To ensure optimal consistency and an up-to-date evidence-based approach over the 4 years of the intervention, treatment recommendations will be offered according to national evidence-based treatment guidelines.
Primary Outcome Measure Information:
Title
Feasibility of the Intervention
Description
The primary end-point for the pilot will be the feasibility of the intervention, measured as follows: A compliance of >=90% with the intervention table on page 17 A success rate (improvement or resolution of problems) of >= 80% A completion rate of >=90% of the initial and final study questionnaires
Time Frame
30 days per participant
Secondary Outcome Measure Information:
Title
Whether the Intervention is Faithful to Dr. McCorkle's Original Intervention
Description
Aim 2 will be judged qualitatively. Dr. Ruth McCorkle and Dr. Janine Overcash will judge whether the intervention is faithful enough to Dr McCorkle's original intervention and whether it can be carried effectively by the trained personnel.
Time Frame
30 days per participant
Title
A Successful Collection and Testing of >=90% of the Samples Tested
Description
Aim 3 will be judged by assessing the percentage of tests that could or not be performed on the Moffitt patients.
Time Frame
30 days per participant
Title
Effect Size Estimates for Within-group Changes Between Baseline and 1-month
Description
Aim 4 will be assessed by the activities of daily living (ADL), instrumental activities of daily living (IADL), complications and FACT-colorectal (FACT-C) v.4 questionnaires at baseline and end of intervention.
Time Frame
30 days per participant

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Colorectal cancer, stage III or IV, confirmed by histology Abdominal surgery by a University of South Florida (USF) surgeon at Moffitt Cancer Center or Tampa General Hospital (TGH) Age 60 years and older Informed consent Living within a one (1) hour radius of Moffitt Exclusion Criteria: Discharge planned to a rehabilitation facility or a nursing home Unable to answer the questionnaires (e.g. because of cognitive impairment, blindness, deafness) Post-operative inpatient stay >one (1) month
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martine Extermann, M.D., Ph.D.
Organizational Affiliation
H. Lee Moffitt Cancer Center and Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
H. Lee Moffitt Cancer Center and Research Institute
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Pilot Study of a Geriatric Intervention After Colorectal and Lung Cancer Surgery

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