PACC: Physical Activity Coaching in Chronic Obstructive Pulmonary Disease (COPD)

Sponsor
Mayo Clinic (Other)
Overall Status
Completed
CT.gov ID
NCT01349608
Collaborator
(none)
50
1
1
23
2.2

Study Details

Study Description

Brief Summary

This study is designed to explore a new approach to help people with chronic obstructive pulmonary disease (COPD) become more physically active. Through weekly telephone sessions with a health coach utilizing motivational interviewing, participants will be empowered to set goals for increased physical activity (emphasis on walking). The objective of the study is to determine if telephone-based health coaching is a reasonable and effective way to increase physical activity, as measured by a gold-standard activity monitor, in people with COPD.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Telephonic health coaching
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Physical Activity Coaching in COPD
Study Start Date :
Apr 1, 2011
Actual Primary Completion Date :
Mar 1, 2013
Actual Study Completion Date :
Mar 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: Health coaching

Behavioral: Telephonic health coaching
Participants will be given a pedometer and activity log to use daily to track their physical activity accomplishments. Weekly, they will participate in a health coaching telephone session to discuss physical activity and set goals. The health coach is knowledgable in COPD care and will utilize a motivational interviewing approach to support the self-efficacy of the participants to be more active.

Outcome Measures

Primary Outcome Measures

  1. Effectiveness of telephone-based health coaching in COPD. [3 Months]

    Determine the effectiveness of a telephone-based health coaching intervention on daily physical activity level, as measured by a gold-standard activity monitor and daily pedometer record, acceptability of intervention through qualitative interviews with participants, and health-related quality of life as measured by questionnaires.

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Men and women age 40 years and older

  • Current or former cigarette smoker of at least 10 pack-years

  • Diagnosis of COPD stage II to IV COPD as documented by pulmonary function testing (FEV1 <80% predicted, FEV1/FVC ration <0.71) within the past 24 months

  • Able to ambulate independently or with a walking aid (wheeled or standard walker or cane)

Exclusion Criteria:
  • Unable to walk without assistance of another person

  • patients with a high likelihood of being lost to follow-up or contact (patients with active chemical dependency), are planning to move out of the state, are not able to be contacted by telephone

  • patients with an inability to provide good data or follow commands (patients who are disoriented or have a severe neurologic/psychiatric condition)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic Rochester Minnesota United States 55905

Sponsors and Collaborators

  • Mayo Clinic

Investigators

  • Principal Investigator: Roberto P Benzo, M.D., MSc, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Roberto P. Benzo, Consultant Pulmonary and Critical Care Medicine, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT01349608
Other Study ID Numbers:
  • 11-000356
First Posted:
May 6, 2011
Last Update Posted:
Apr 4, 2013
Last Verified:
Apr 1, 2013
Keywords provided by Roberto P. Benzo, Consultant Pulmonary and Critical Care Medicine, Mayo Clinic
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 4, 2013