N/A N=60 Randomized Single-blind Supportive Care

I-STAND R21: Reducing Sedentary Time in Older Adults

Obesity · Sedentary Lifestyle

Bottom Line

View on ClinicalTrials.gov: NCT02692560 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

May 2018

Primary outcome: Primary: Change in Hours of Sitting Time — -70.1; 6.5 minutes

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: I-STAND (Behavioral); Healthy Living (Other)
Age: Adult, Older Adult · 60+ yrs
Sex: All
Sponsor: Kaiser Permanente
Primary completion: Feb 2017

Outcome Measures

Outcome	Result	p-value
PRIMARY Change in Hours of Sitting Time	-70.1; 6.5	—
SECONDARY Sit-to-stand Transitions	-0.1; 2.2	—
SECONDARY Periods of Sitting for 30+ Minutes	-2.5; 0.1	—
SECONDARY Physical Function	-0.5; 0.2	—
SECONDARY Blood Pressure (Systolic Blood Pressure)	-3.4; -1.5	—
SECONDARY Fasting Glucose (mg/dL)	8.8; 2.4	—
SECONDARY Total Cholesterol (mg/dL)	6.0; 0.4	—
SECONDARY Depressive Symptoms	-1.0; -0.6	—

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.

Eligibility Criteria

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

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02692560). 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.