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I-STAND R21: Reducing Sedentary Time in Older Adults

Not Applicable
Completed
Conditions
Sedentary Lifestyle
Obesity
Interventions
Other: Healthy Living
Behavioral: I-STAND
Registration Number
NCT02692560
Lead Sponsor
Kaiser Permanente
Brief Summary

The investigators are doing a study to learn how to support patients aged 60+ in taking more breaks from sitting and reducing total sitting time. The goal of the study is to find out if a sitting time reduction intervention reduces sitting time compared with a control group.

Detailed Description

More than one-third of American adults over 60 have a body mass index \> 30 kg/m2. These older adults have more sedentary time than any other group -- an average of 10-11 hours per day. Reducing the sedentary behavior of older adults with obesity, rather than only promoting more intensive physical activity, could provide a more feasible approach to health promotion.

This randomized control pilot trial will evaluate a 12-week intervention to decrease sitting time and increase standing time and light physical activity among sedentary older adults a body mass index \> 30 kg/m2 as compared to control group. Baseline and 12-week measurements include anthropometric measures, blood draw by finger stick, cardiovascular health assessments, physical function tasks, and a survey. The intervention will consist of two in-person visits with a health coach followed by phone-based coaching.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Kaiser Permanente Washington enrollees
  • Men and women
  • Age 60 - 89
  • BMI 30 - 50 (calculated based on most recent height ever and most recent weight taken within previous 18 months)
  • Primary care within Integrated Group Practice
  • Continuously enrolled at Kaiser Permanente Washington for previous 12 months
  • No record of death
  • Not on the No Contact list
  • Speaks and writes English
  • Able to hold a conversation by phone (no hearing or other limitations)
  • Self-reported sitting time of 6 hours/day or more
  • Self-reported ability to stand with or without an assistive device
  • Self-reported ability to walk one block with or without an assistive device
  • Available for the study duration
  • Able to come to Kaiser Permanente Washington Health Research Institute's research clinic for measurement visits
  • Willing to wear study activity monitors
Exclusion Criteria
  • Resides in long-term care, hospice care, or skilled nursing facility (previous 12 months)
  • Wheelchair bound
  • Diagnosis of dementia, serious mental health disorder, or substance use disorder (previous 24 months)
  • Use of an assistive device

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Healthy LivingHealthy LivingParticipants randomly assigned to the Healthy Living enhanced usual care control group will receive 1 in-person health coaching session and 5 biweekly check-in letters by mail. They will receive a workbook with general healthy living topics that are not expected to impact sitting time. All content is taken from Kaiser Permanente Washington's website and is available to all members. Participants will select topics of interest and review them on their own with no further health coaching.
I-STANDI-STANDParticipants randomly assigned to the I-STAND intervention group will receive 2 in-person health coaching sessions and 4 biweekly phone-based health coaching sessions. They will receive a wristband that gives a mild vibration after 20 minutes of inactivity and will be encouraged to stand if possible after each inactivity alert. Participants may also choose to receive biweekly email reminders in the weeks between coaching calls. They will also receive a workbook with content around reducing sitting time.
Primary Outcome Measures
NameTimeMethod
Change in Hours of Sitting Time12 weeks

Average hours of sitting time over the last 7 days measured at baseline and 12 weeks later

Secondary Outcome Measures
NameTimeMethod
Physical Function12 weeks

Change in Short Physical Performance Battery (SPPB) scale score, from baseline to 12 weeks. The range of scores is 0 to 12, higher values represent better physical function.

Sit-to-stand Transitions12 weeks

Change in average daily number of activPAL-measured sit-to-stand transitions, from baseline to 12 weeks

Periods of Sitting for 30+ Minutes12 weeks

Change in average daily number of activPAL-measured periods of sitting for 30+ minutes without standing, from baseline to 12 weeks

Blood Pressure (Systolic Blood Pressure)12 weeks

Change in average of second and third blood pressure reading (for systolic blood pressure), from baseline to 12 weeks

Depressive Symptoms12 weeks

Change in Patient Health Questionnaire (PHQ-8) scale score, from baseline to 12 weeks. The scale range is 0 to 24 with higher scores representing higher depressive symptoms. Scores of 10 or more are considered major depression.

Fasting Glucose (mg/dL)12 weeks

Change in fasting glucose (mg/dL) from finger stick blood draw, from baseline to 12 weeks

Total Cholesterol (mg/dL)12 weeks

Change in total cholesterol (mg/dL) from finger stick blood draw, from baseline to 12 weeks

Trial Locations

Locations (1)

Kaiser Permanente Washington Health Research Institute

🇺🇸

Seattle, Washington, United States

Kaiser Permanente Washington Health Research Institute
🇺🇸Seattle, Washington, United States
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