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Exercise Training Study for Patients With Cystic Fibrosis

Primary Purpose

Cystic Fibrosis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Self-Regulated Exercise with Telephone Reinforcement
Standard Treatment
Qualitative Approach
Sponsored by
University of Pittsburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cystic Fibrosis focused on measuring cystic fibrosis, exercise, perceived exertion, aerobic fitness, lung function, health related quality of life, self-regulated exercise

Eligibility Criteria

10 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • CF diagnosis
  • age 10-18 years
  • reliable pulmonary function tests
  • living at home
  • able to read
  • able to ride a stationary bike
  • able to walk and/or run on a treadmill.

Exclusion Criteria:

  • Enrolled in another intervention study
  • in structured aerobic activity for 30 continuous minutes 3 times per week
  • sibling enrolled in study.

Sites / Locations

  • Antiono J & Janet Palumbo Cystic Fibrosis Center; Children's Hospital of Pittsburgh of UPMC

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

Self-Regulated Exercise with Telephone Reinforcement

Attention Control

Outcomes

Primary Outcome Measures

Cardiopulmonary Fitness: Peak VO2

Secondary Outcome Measures

Cardiopulmonary fitness: VO2150 and peak power output
Pulmonary function: FEV1 and sustained phonation time
Health-related quality of life: Quality of well-being scale and cystic fibrosis questionnaire
Exercise experiences of children and parents: Interviews

Full Information

First Posted
January 31, 2008
Last Updated
February 18, 2016
Sponsor
University of Pittsburgh
Collaborators
National Institute of Nursing Research (NINR)
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1. Study Identification

Unique Protocol Identification Number
NCT00609050
Brief Title
Exercise Training Study for Patients With Cystic Fibrosis
Official Title
Self-Regulated Exercise in CF: A Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Completed
Study Start Date
March 2007 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh
Collaborators
National Institute of Nursing Research (NINR)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to test the effect of a 6-month program of self-regulated, home-based exercise with telephone reinforcement on the cardiorespiratory fitness, pulmonary function and health-related quality of life of children with cystic fibrosis (CF), compared to controls. Exploring the exercise experiences of the children and parents is a secondary aim.
Detailed Description
CF is a life-long illness that requires complex and dynamic adjustment by the patient and family. The nursing role is vital to the multidisciplinary team approach required in providing comprehensive, individualized care for these patients. Nurses facilitate the coordination of health care efforts and support the patient and family across physical and psychosocial domains. With the well-documented correlation between exercise tolerance and both survival and HRQoL, exercise represents a critical treatment focus for CF patients. Nurses contribute to standard exercise rehabilitation programs, through education, psychosocial support, and communication. In this exercise training study, the nursing role will include: a) teaching the patients and families how to use the OMNI scale, b) confirming that they understand the home-based exercise regimen, and c) ensuring that the home-care program is properly followed by placing weekly telephone calls to assess progress and barriers. Long-term nursing application will occur via dissemination of the OMNI training manual, to be developed as part of this study, for use by CF nurses in clinics worldwide.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis
Keywords
cystic fibrosis, exercise, perceived exertion, aerobic fitness, lung function, health related quality of life, self-regulated exercise

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
38 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Self-Regulated Exercise with Telephone Reinforcement
Arm Title
2
Arm Type
Active Comparator
Arm Description
Attention Control
Intervention Type
Behavioral
Intervention Name(s)
Self-Regulated Exercise with Telephone Reinforcement
Intervention Description
The self-regulated exercise with telephone reinforcement group will engage in a three-times-a-week (or more) at home exercise regimen for 6 months during which they may choose the mode of exercise. They will receive weekly telephone calls about exercise and airway clearance. After 6 months, they will be instructed to maintain their self-regulated exercise activity for the remaining 6 months of the study, but they will not receive telephone calls
Intervention Type
Behavioral
Intervention Name(s)
Standard Treatment
Intervention Description
The attention control group will receive standard recommendations for exercise activity, during the first 6 months, as is common in our clinic. Also during the first 6 months, they will receive weekly telephone calls about airway clearance. For the final 6 months of the study, the attention control group will cross over to self-regulated exercise without telephone reinforcement.
Intervention Type
Behavioral
Intervention Name(s)
Qualitative Approach
Intervention Description
A qualitative naturalistic approach is nested within the primary experimental framework to explore the experiences of the children and parents, in both groups, with the exercise regimen.
Primary Outcome Measure Information:
Title
Cardiopulmonary Fitness: Peak VO2
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Cardiopulmonary fitness: VO2150 and peak power output
Time Frame
1 year
Title
Pulmonary function: FEV1 and sustained phonation time
Time Frame
1 year
Title
Health-related quality of life: Quality of well-being scale and cystic fibrosis questionnaire
Time Frame
1 Year
Title
Exercise experiences of children and parents: Interviews
Time Frame
1 Year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: CF diagnosis age 10-18 years reliable pulmonary function tests living at home able to read able to ride a stationary bike able to walk and/or run on a treadmill. Exclusion Criteria: Enrolled in another intervention study in structured aerobic activity for 30 continuous minutes 3 times per week sibling enrolled in study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David M Orenstein, MD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Antiono J & Janet Palumbo Cystic Fibrosis Center; Children's Hospital of Pittsburgh of UPMC
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Exercise Training Study for Patients With Cystic Fibrosis

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