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NCT02082223 Clinical Trial

Individualized Preoperative Rehabilitation Pilot

Quality of Life Clinical Trial

— iPREHAB  

Official title:
Individualized Preoperative Rehabilitation (iPREHAB) Pilot

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02082223
Other study ID # 13-005601
Secondary ID
Status Completed
Phase N/A
First received March 6, 2014
Last updated February 27, 2018
Start date March 2014
Est. completion date December 25, 2017

Study information
Verified date February 2018
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A pilot to test feasibility of improving patient/caretaker quality of life and resilience.

Description:

Our overall goal is to investigate if pre-operative interventions can address patients' and patients' care givers quality of life/resilience deficits and thus improve outcomes. This initial pilot study will test the feasibility of offering patients and their care givers prehabilitation interventions prior to complex gastrointestinal surgery such as pancreatectomy, esophagectomy, proctectomy, or hepatectomy.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date December 25, 2017
Est. primary completion date June 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 99 Years
Eligibility 1. Patients who are being seen for pancreatic, esophageal, rectal or hepatic neoplastic disease, will undergo neo-adjuvant therapy and may require complex GI surgery and their care givers.

2. Are able and willing to participate in all aspects of the study; and

3. Have been provided with, understand the consent.

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Interventions to improve preop QOL/resilience deficits
Identify patients' and patients' care givers quality of life/resilience deficits and supply information and resources prior to undergoing complex GI surgery.

Locations
Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Feasibility Primary outcome is the feasibility of the interventions as measured through the end of study feedback form. 3 months post surgical
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