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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01593449
Other study ID # NIH 5 UL1RR031982-02
Secondary ID
Status Completed
Phase Phase 1
First received April 30, 2012
Last updated April 11, 2013
Start date January 2011
Est. completion date December 2012

Study information

Verified date April 2013
Source University of Massachusetts, Worcester
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The present study aims to initially test a community dog walking intervention that addresses individual, interpersonal and community factors associated with dog walking. The study will be conducted in two cities, Worcester and Lowell, as a collaboration between investigators from UMass Medical School and UMass-Lowell.


Description:

This is a group randomized trial where 8 communities in Worcester and Lowell (4 per city) will be randomly assigned to the 6-month dog walking intervention or a standard, self-help, print-based physical activity control condition. Dog owners (N=120; 15 per community) will be recruited. The intervention includes a social networking website, monthly newsletters, twice monthly neighborhood dog walks and community events. The intervention will: 1) educate owners about the benefits of dog walking to themselves and their dog, 2) teach strategies for regular dog walking, 3) teach dog walking tips and provide dog training seminars, 4) promote self-monitoring and goal setting for dog walking, 5) provide social networking opportunities for dog owners and 6) promote a sense of community via participation in neighborhood dog walks and community events. Intervention feasibility will be assessed by measures of implementation success, including recruitment and retention rates, website use, intervention satisfaction and attendance at neighborhood walks and community events. Initial efficacy will be assessed via change in weekly steps measured via a pedometer from baseline to 6-months after baseline.


Recruitment information / eligibility

Status Completed
Enrollment 107
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 21 Years and older
Eligibility Inclusion Criteria:

- Eligible participants will own a dog that is in good health and considered a household pet, be a Worcester or Lowell resident, be aged > 21 years old and have home internet access. Participants with cardiovascular disease, diabetes or other chronic health condition are eligible with permission from their PCP to participate.

Exclusion Criteria:

Participants will be excluded for any of the following:

1. Inability or unwillingness to give informed consent

2. Plans to move out of the area within the study period

3. Participated in a focus group during the developmental phase

4. Another household member is participating in the study

5. Pregnant or planning a pregnancy in the next six months

6. Condition that inhibits exercise (e.g., unable to walk unaided, or cannot walk 1/4 mile without stopping)

7. Incapable of engaging in physical activity as assessed by the Physical Activity Readiness Questionnaire

8. Self-report engaging in > 150 minutes of moderate and vigorous intensity physical activity per week.

9. The participant's dog has a history of biting a human or has not received a rabies vaccination.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
Community-based social networking intervention
Participation in this study lasts for 7 months and includes a baseline visit, an orientation visit, the 6 month intervention, and a 6 month assessment visit.

Locations

Country Name City State
United States University of Massachusetts Lowell Lowell Massachusetts
United States University of Massachusetts Medical Schol Worcester Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
University of Massachusetts, Worcester University of Massachusetts, Lowell

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary feasibility Feasibility will be assessed by implementation success, including recruitment and retention rates, website use, intervention satisfaction and attendance at neighborhood walks and community events. 6 months No
Secondary Weekly steps Pedometers that record 7-days of data will be used to measure steps at baseline and 6 months baseline and 6 months No
Secondary weekly dog walking minutes Self-reported minutes of dog walking measured using the DAPA tool. baseline and 6 months No
Secondary social support for walking Self-reported social support for walking baseline and 6 months No
Secondary sense of community self-reported sense of community baseline and 6 months No
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