No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
65 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
3,000 (estimated)
Sponsor
The Cleveland Clinic · Other
Who this trial is looking for
This trial is looking for older patients who are in the hospital and may benefit from guided walking sessions. Participants will either receive this walking program or standard care during their hospital stay.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 65 years old
I am currently in the hospital for medical care
I have a complete medical history on file
I have a 6-Clicks score of 16-23
I have insurance through Medicare or Medicare Advantage
You may not be able to join if
I need a translator due to a language barrier
I am being discharged today or tomorrow
I am in observation status
I have a planned surgery
I have unstable angina or another condition preventing exercise
I live permanently in a nursing facility
I am only receiving comfort care
I have been in the hospital for more than 48 hours
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The investigator proposes to conduct a randomized trial of supervised ambulation delivered by mobility technician (MT) up to three times daily, including weekends, to hospitalized medical patients. The aims of the study are to compare the short and intermediate-term outcomes of patients randomized to the intervention versus those patients randomized to receive usual care, to identify patients who …
The investigator proposes to conduct a randomized trial of supervised ambulation delivered by mobility technician (MT) up to three times daily, including weekends, to hospitalized medical patients. The aims of the study are to compare the short and intermediate-term outcomes of patients randomized to the intervention versus those patients randomized to receive usual care, to identify patients who are most likely to benefit from the intervention and to assess whether the intervention increases or decreases overall costs of an episode of care, including the cost of the MTs, the index hospitalization and the first 30 days post enrollment.
Trial Locations
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City
State
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Status
Eligibility Criteria
Inclusion Criteria:
Participants must meet all of the inclusion criteria listed below to participate in this study:
1. ≥65 years of age
2. Admitted to a medical service
3. Complete history and physical examination on file
4. 6-Clicks score of 16-23
5. Insurance with Traditional Medicare or Medicar…
Inclusion Criteria:
Participants must meet all of the inclusion criteria listed below to participate in this study:
1. ≥65 years of age
2. Admitted to a medical service
3. Complete history and physical examination on file
4. 6-Clicks score of 16-23
5. Insurance with Traditional Medicare or Medicare Advantage
Exclusion Criteria:
Any patient meeting any of the exclusion criteria listed below at baseline will be excluded from study participation:
1. Significant language barrier that requires a translator (other than Spanish at Baystate site only)
2. Discharge planned for that day or the following day
3. Observation status
4. Surgical procedure planned
5. Patients diagnosed with unstable angina or other medical conditions precluding participation in exercise/ambulation
6. Permanent residence in a skilled nursing facility
7. Comfort care measures only
8. \>48 hours since admission
9. Active infection with COVID-19
10. Other active infection requiring contact or droplet precautions
11. Order for bedrest
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