N/A
N=38
Reducing Sedentary Behavior vs. Increasing Physical Activity in Older Adults
Sedentary Lifestyle
Bottom Line
View on ClinicalTrials.gov: NCT02146001 ↗Enrolled (actual)
38
Serious AEs
0.0%
Results posted
Aug 2016
Primary outcome: Primary: Change in Objectively Monitored Sedentary Behavior — -0.1; 0.6 hours/day
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Reducing sedentary behavior group (Other); Moderate-to-vigorous activity group (Other)
- Age
- Adult, Older Adult · 60+ yrs
- Sex
- All
- Sponsor
- University of Pittsburgh
- Primary completion
- Nov 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Objectively Monitored Sedentary Behavior |
-0.1; 0.6 | — |
| SECONDARY Change in Physical Function (Short Physical Performance Battery [SPPB]) |
0.2; 0.5 | — |
| SECONDARY Change in Objectively-monitored Moderate-to-vigorous Physical Activity |
75; -7 | — |
Summary
This study is a randomized trial that will compare the effects of two, 12-week activity interventions on patterns of physical activity, physical health, and quality of life measures in 40 older adults who are able to walk for exercise. One intervention will target 150 minutes per week of home-based moderate exercise (e.g. brisk walking), consistent with current recommendations. The other intervention will target a decrease in time spent in sedentary behaviors (e.g. sitting) of 60 minutes per day. Both interventions will wear an activity armband which will allow them to self-monitor their activity or sedentary behavior in real time using a smartphone. The armband will also provide objective data to an interventionist that will facilitate the intervention. The main outcome will be time spent in moderate exercise.
Eligibility Criteria
Inclusion Criteria
- Age ≥60 years
- Currently engage in 3 alcoholic beverages per day
Data sourced from ClinicalTrials.gov (NCT02146001). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.