Skip to main content
OpenTrials
Completed

NCT Number: NCT03299504

Factors Predicting Success in Lung Transplant Recipients Who Have Undergone Intensive Post-operative Rehabilitation

This is a retrospective review of the COLTT program outcomes and factors that predict recovery of functional status after lung transplantation.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

IU Health Methodist Hospital

Indianapolis, Indiana, 46202, United States

About this study

The Center of Life for Thoracic Transplant (COLTT) program is a daily (5 days per week) intensive rehabilitation program for patients who have undergone lung transplant. Patients are enrolled in COLTT as part of standard care after hospital discharge. This study is a retrospective review of seventy patients that measures the efficacy of the COLTT program and establishes predictors of patient success.This study will also measure the effect of functional outcomes on hospital readmission post COLTT discharge.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients who completed the COLTT program from May, 2016 to July, 2017.

Exclusion criteria

  • Any COLTT patients who were not new lung transplant recipients.

Treatment and study plan

Exercise

Other

5 days per week, 2.5 hours per day strength, balance and endurance training on an outpatient basis

Primary outcomes

  1. Time to reach program goals (days)

    Time frame: Through study completion, an average of 4 weeks

    The number of days in the COLTT program required to reach program goals ( see secondary outcomes measures)

Secondary outcomes

  1. Gait speed (mph, % expected)

    Time frame: Through study completion, an average of 4 weeks

    Gait speed (walking speed) is measured daily on a oval track

  2. Single leg stance performance (seconds, % expected)

    Time frame: Through study completion, an average of 4 weeks

    The test result of a single leg stance test. Patients stand with hands on their hips, raise one leg off the ground and hold it for as long as possible.

  3. One-minute sit to stand performance (number, % expected)

    Time frame: Through study completion, an average of 4 weeks

    The test result of a one-minute sit to stand test. Patients stand/sit from a chair as many times as they can in one minute.

  4. Six minute walk distance (feet, % expected)

    Time frame: Through study completion, an average of 4 weeks

    The test result of a six-minute walk test, a field test of exercise capacity

Other outcomes

  1. Hospital readmission

    Time frame: 6 months

    Measured as number of hospital readmissions

Sponsors and collaborators

Lead sponsor

Indiana University Health Methodist Hospital

Other

Registry information

Official study title

Factors Predicting Success in Lung Transplant Recipients Who Have Participated in the COLTT Program (Daily Intensive Post-hospitalization Rehabilitation): A Retrospective Review

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Oct 3, 2017
Registry last updated
Aug 24, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed

Planned Semi-Elective Lung Tx Study

NCT04601818

Lung Transplant, To Compare Lung Transplant Outcomes Between Study Patients and Standard Patients Who Have Already Undergone Lung Transplantation by Conventional Procedures

Gainesville, Florida, United States

View Trial Details