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Behavioral Intervention

Intervention Group for Frailty Syndrome (OASIS Trial)

N/A
Waitlist Available
Led By Jens M Walz, MD
Research Sponsored by University of Massachusetts, Worcester
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 7-10 weeks (baseline can be anywhere between 3 to 6 weeks pre-surgery, therefore 4 weeks post surgery can be anywhere from 7 weeks after baseline to 10 weeks after baseline)
Awards & highlights

OASIS Trial Summary

This trial found that pre-operative remote coaching and a walking plan improved post-operative mobility and stamina in frail older adults.

OASIS Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~7-10 weeks (baseline can be anywhere between 3 to 6 weeks pre-surgery, therefore 4 weeks post surgery can be anywhere from 7 weeks after baseline to 10 weeks after baseline)
This trial's timeline: 3 weeks for screening, Varies for treatment, and 7-10 weeks (baseline can be anywhere between 3 to 6 weeks pre-surgery, therefore 4 weeks post surgery can be anywhere from 7 weeks after baseline to 10 weeks after baseline) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
6 Minute Walk Distance
Secondary outcome measures
6MWD baseline to presurgical appointment day
Baseline to 4 weeks post surgery 6MWD
Change in The Veterans Rand 12-Item Health Survey (VR12), baseline to 4 wks and 6 months
+1 more

OASIS Trial Design

3Treatment groups
Experimental Treatment
Active Control
Group I: Intervention GroupExperimental Treatment1 Intervention
Participants are prescribed a walking prescription based on their baseline daily step count. During the interim between the day of consultation until the day of surgery, a study staff member will make weekly calls to each participant. Participants will also log all of their physical activities including the date, activity type, and number of minutes.
Group II: Observation GroupActive Control1 Intervention
Participants who are not frail will receive usual care prior to surgery and charts will be reviewed for outcomes following surgery.
Group III: Control GroupActive Control1 Intervention
Participants receive usual care prior to surgery. Participants will also log all of their physical activities including the date, activity type, and number of minutes.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Intervention Group
2020
Completed Phase 2
~7240

Find a Location

Who is running the clinical trial?

Anesthesia Patient Safety FoundationOTHER
10 Previous Clinical Trials
3,550 Total Patients Enrolled
University of Massachusetts, WorcesterLead Sponsor
342 Previous Clinical Trials
976,430 Total Patients Enrolled
Jens M Walz, MDPrincipal InvestigatorUniversity of Massachusetts, Worcester

Frequently Asked Questions

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

Is there still availability to join this research project?

"Clinicaltrials.gov reports this research is no longer actively recruiting participants, though it was initially launched on March 1st 2019 and last updated in July 12th 2022. However, there are currently 19 additional studies looking for volunteers now."

Answered by AI
~30 spots leftby Apr 2025