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Sedentary behavior reduction intervention for Sedentary Lifestyle

N/A
Waitlist Available
Led By Olga Theou, PhD
Research Sponsored by Olga Theou
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from baseline up to 30 days after hospital discharge
Awards & highlights

Study Summary

This trial will compare whether reducing sedentary time for patients in acute care results in less frailty at discharge, compared to the current standard of care. All patients will wear accelerometers, then be randomly assigned to a control or intervention group. The control group will only receive standard of care while in hospital. Participants in the intervention group will have daily goals for time out-of-bed, and receive feedback on a bedside monitor. If participants in the intervention group haven't met their daily goal by late afternoon, they'll receive assisted mobilization. The main outcome is frailty, assessed by a frailty index.

Eligible Conditions
  • Sedentary Lifestyle

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline frailty up to a median 14 days hospital length of stay, and 30 days after hospital discharge
This trial's timeline: 3 weeks for screening, Varies for treatment, and change from baseline frailty up to a median 14 days hospital length of stay, and 30 days after hospital discharge for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Secondary outcome measures
Change in balance: Hierarchical Assessment of Balance and Mobility (HABAM)
Change in mobility: Hierarchical Assessment of Balance and Mobility (HABAM)
Change in the Frailty Index
+8 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention GroupExperimental Treatment1 Intervention
Fitted with accelerometer to measure time spent out of bed while in hospital; daily goals set for time spent out of bed; mobilization feedback real-time feedback on goal attainment; hands on mobilization by physiotherapist for participants in late afternoon for participants who do not meet daily goal.
Group II: Control GroupActive Control1 Intervention
Fitted with an accelerometer to measure time spent out of bed while in hospital. Otherwise, participants in the control group will receive usual care from the hospital medical team during their hospital stay. Daily activities of participants will not be restricted if patients are assigned to the control group.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Sedentary behavior reduction intervention
2022
N/A
~50

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Who is running the clinical trial?

Olga TheouLead Sponsor
1 Previous Clinical Trials
50 Total Patients Enrolled
Olga Theou, PhDPrincipal InvestigatorAssistant Professor, Department of Medicine, Dalhousie University

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

How many participants are being evaluated as part of this research?

"Affirmative. Data hosted on clinicaltrials.gov confirms that this medical research, which was first posted on April 7th 2022, is actively recruiting. About 50 patients need to be recruited from a single site."

Answered by AI

Are there any openings available for enrolment in this research trial?

"Affirmative. Data found on clinicaltrials.gov verifies that this investigation, which was first advertised on April 7th 2022 is currently enrolling participants. Approximately 50 people are needed to be enrolled from a single medical facility."

Answered by AI
Recent research and studies
~17 spots leftby Apr 2025