Utilizing Tailored Step-Count Feedback to Enhance Physical Activity in the Elderly (StepCount)
This study is currently recruiting participants.
Verified July 2012 by University of Wisconsin, Milwaukee
Sponsor:
University of Wisconsin, Milwaukee
Collaborator:
Information provided by (Responsible Party):
Scott J. Strath, University of Wisconsin, Milwaukee
ClinicalTrials.gov Identifier:
NCT01158638
First received: July 7, 2010
Last updated: July 10, 2012
Last verified: July 2012
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Purpose
Individually tailored, mediated pedometer feedback will provide an effective method to promote physical activity adoption in the elderly
| Condition | Intervention | Phase |
|---|---|---|
|
Physical Activity Elderly |
Behavioral: Web Mediated Step Intervention |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Single Group Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Utilizing Tailored Step-Count Feedback to Enhance Physical Activity in the Elderly |
Further study details as provided by University of Wisconsin, Milwaukee:
Primary Outcome Measures:
- Objectively assessed steps per day [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]Pedometer determined physical activity
| Estimated Enrollment: | 160 |
| Study Start Date: | August 2009 |
| Estimated Study Completion Date: | December 2012 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
No Intervention: Usual Care
Usual Care
|
|
|
Active Comparator: 10,000 Steps Group
Each participant randomized to this study arm will receive a pedometer and a generic recommendation to accumulate 10,000 Steps per Day.
|
Behavioral: Web Mediated Step Intervention
The testing of a web mediated step intervention designed to set weekly step targets, and channel participants through a series of motivational screens depending on compliance or non-compliance with set step goals.
|
|
Experimental: Web Mediated Step Group
Participants randomized to this study arm receive an introduction to the study website. Each person utilizes the website to track their daily physical activity steps. Goals are given on a weekly basis to increase steps by 10% per day per week over baseline values. The website channels each participant through a series of motivational messages designed to increase compliance with recommended physical activity targets
|
Behavioral: Web Mediated Step Intervention
The testing of a web mediated step intervention designed to set weekly step targets, and channel participants through a series of motivational screens depending on compliance or non-compliance with set step goals.
|
Eligibility| Ages Eligible for Study: | 50 Years to 85 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Male or female individuals living in the community.
- Aged between 50 and 85 years, at screening.
Sufficient physical function not to have limitations to participate in physical activity demonstrated by:
- Habitual gait speed ≥ 1.5 mph, AND
- No use of a cane or walker, AND
- Able to walk ≥ 50 feet unaided
- Sufficient cognitive function, as demonstrated by responses to the mini-mental state examination(>23 score).
- Be able to read and write in English
- Sedentary behavior, demonstrated by no regular activity / exercise for previous 6 months and/or a Stage of Change 2 and 3
Exclusion Criteria:
- Presence of a rapidly progressive or terminal illness condition that is expected to result in significant functional decline during the course of the proposed studies.
- Significant uncontrolled cardiovascular disease and conditions, e.g. unstable or new onset angina, unrepaired aortic aneurysms, critical aortic stenosis or CAD without bypass, persistent moderate to severe uncontrolled hypertension.
- Significant uncontrolled metabolic disease, e.g. hemoglobin A1c levels greater than 8.0 and/or glucose levels greater than 300 mg/dL.
- Fracture of lower extremity within three months.
- Amputation other than toes.
- Current history of severe arthritis or orthopedic condition precluding physical activity.
- Participation in any regular structured exercise (resistance training, Tai Chi, high intensity walking, jogging, cycling, stair climbing, stepping, within the previous 6 months.
- Individuals that start a new medication that can impact health variables examined during study period (e.g., beta blockers, glucose or cholesterol altering medications), or individuals who alter medication dose that can impact health variables examined within study period.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01158638
Contacts
| Contact: Nora E Miller, M.S. | 414 229 4352 | nem2@uwm.edu |
Locations
| United States, Wisconsin | |
| Physical Activity & Health Research Laboratory | Recruiting |
| Milwaukee, Wisconsin, United States, 53201 | |
| Contact: Nora e Miller, M.S. 414-229-4352 nem2@uwm.edu | |
| Principal Investigator: Scott J Strath, PhD | |
Sponsors and Collaborators
University of Wisconsin, Milwaukee
Investigators
| Principal Investigator: | Scott J Strath, PhD | University of Wisconsin, Milwaukee |
More Information
No publications provided
| Responsible Party: | Scott J. Strath, Associate Professor, University of Wisconsin, Milwaukee |
| ClinicalTrials.gov Identifier: | NCT01158638 History of Changes |
| Other Study ID Numbers: | StepCount, K01AG025962 |
| Study First Received: | July 7, 2010 |
| Last Updated: | July 10, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of Wisconsin, Milwaukee:
|
Physical Activity Enhancement |
ClinicalTrials.gov processed this record on May 19, 2013