Trial Outcomes & Findings for Pilot Randomized Controlled Study of the Impact of MedRhythms' MR-010 in Acute Stroke (NCT NCT04689256)

NCT ID: NCT04689256

Last Updated: 2025-01-08

Results Overview

Change in gait speed (m/s) from baseline to study completion as measured by a 6 meter walking test.

Recruitment status

TERMINATED

Study phase

NA

Target enrollment

4 participants

Primary outcome timeframe

90 days

Results posted on

2025-01-08

Participant Flow

Recruited in hospital after confirmed diagnosis of acute stroke from 11/03/2021 to 11/27/2022. Study terminated due to lower than expected recruitment

Patients included following diagnosis of acute stroke

Participant milestones

Participant milestones
Measure
MR-010 Walking Therapy
Subjects will use the MR-010 three times a week for 30 minutes per session for 90 days. Subjects will undergo a 10-meter walk test bi-weekly and at 45 and 90 days. MR-010: MR-010 includes a patient application and sensors with commercially available headphones and smartphones. Sensors are placed on the subject's shoes and measure gait metrics. The algorithm uses data from the sensors to inform changes made to the audio cues. These cues, which are embedded in time-shifted music, are delivered back to the users who aim to walk to the beat.
Standard of Care
Subjects will undergo a 10-meter walk test bi-weekly for 90 days and at 45 and 90 days
Overall Study
STARTED
2
2
Overall Study
COMPLETED
0
2
Overall Study
NOT COMPLETED
2
0

Reasons for withdrawal

Reasons for withdrawal
Measure
MR-010 Walking Therapy
Subjects will use the MR-010 three times a week for 30 minutes per session for 90 days. Subjects will undergo a 10-meter walk test bi-weekly and at 45 and 90 days. MR-010: MR-010 includes a patient application and sensors with commercially available headphones and smartphones. Sensors are placed on the subject's shoes and measure gait metrics. The algorithm uses data from the sensors to inform changes made to the audio cues. These cues, which are embedded in time-shifted music, are delivered back to the users who aim to walk to the beat.
Standard of Care
Subjects will undergo a 10-meter walk test bi-weekly for 90 days and at 45 and 90 days
Overall Study
Participants declined to participate in the interventions per protocol
2
0

Baseline Characteristics

Pilot Randomized Controlled Study of the Impact of MedRhythms' MR-010 in Acute Stroke

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
MR-010 Walking Therapy
n=2 Participants
Subjects will use the MR-010 three times a week for 30 minutes per session for 90 days. Subjects will undergo a 10-meter walk test bi-weekly and at 45 and 90 days. MR-010: MR-010 includes a patient application and sensors with commercially available headphones and smartphones. Sensors are placed on the subject's shoes and measure gait metrics. The algorithm uses data from the sensors to inform changes made to the audio cues. These cues, which are embedded in time-shifted music, are delivered back to the users who aim to walk to the beat.
Standard of Care
n=2 Participants
Subjects will undergo a 10-meter walk test bi-weekly for 90 days and at 45 and 90 days
Total
n=4 Participants
Total of all reporting groups
Age, Categorical
<=18 years
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Age, Categorical
Between 18 and 65 years
0 Participants
n=5 Participants
1 Participants
n=7 Participants
1 Participants
n=5 Participants
Age, Categorical
>=65 years
2 Participants
n=5 Participants
1 Participants
n=7 Participants
3 Participants
n=5 Participants
Age, Continuous
66.5 years
n=5 Participants
67.5 years
n=7 Participants
67 years
n=5 Participants
Sex: Female, Male
Female
0 Participants
n=5 Participants
1 Participants
n=7 Participants
1 Participants
n=5 Participants
Sex: Female, Male
Male
2 Participants
n=5 Participants
1 Participants
n=7 Participants
3 Participants
n=5 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
2 Participants
n=5 Participants
2 Participants
n=7 Participants
4 Participants
n=5 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
Asian
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
Black or African American
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
White
2 Participants
n=5 Participants
2 Participants
n=7 Participants
4 Participants
n=5 Participants
Race (NIH/OMB)
More than one race
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
n=5 Participants
0 Participants
n=7 Participants
0 Participants
n=5 Participants
Region of Enrollment
United States
2 participants
n=5 Participants
2 participants
n=7 Participants
4 participants
n=5 Participants

PRIMARY outcome

Timeframe: 90 days

Population: No subjects completed the at home 6 Meter Walking Test. Therefore, no data was collected for this outcome measure.

Change in gait speed (m/s) from baseline to study completion as measured by a 6 meter walking test.

Outcome measures

Outcome data not reported

PRIMARY outcome

Timeframe: 90 days

Population: Data for this outcome was only intended to be collected and measured for participants in the MR-010 walking therapy group. As no participants completed the MR-101 walking therapy intervention, no data was collected.

Adherence to the MR-010 therapy schedule is measured by the number of participants who completed scheduled sessions (3 times per week for 12 weeks)

Outcome measures

Outcome data not reported

SECONDARY outcome

Timeframe: Duration of hospital stay, up to 14 days

Median length of stay in acute stroke hospital

Outcome measures

Outcome measures
Measure
MR-010 Walking Therapy
n=2 Participants
Subjects will use the MR-010 three times a week for 30 minutes per session for 90 days. Subjects will undergo a 10-meter walk test bi-weekly and at 45 and 90 days. MR-010: MR-010 includes a patient application and sensors with commercially available headphones and smartphones. Sensors are placed on the subject's shoes and measure gait metrics. The algorithm uses data from the sensors to inform changes made to the audio cues. These cues, which are embedded in time-shifted music, are delivered back to the users who aim to walk to the beat.
Standard of Care
n=2 Participants
Subjects will undergo a 10-meter walk test bi-weekly for 90 days and at 45 and 90 days
Length of Stay
3 days
Interval 2.0 to 4.0
3 days
Interval 2.0 to 4.0

SECONDARY outcome

Timeframe: 90 days

Percent of readmission to hospital following discharge

Outcome measures

Outcome measures
Measure
MR-010 Walking Therapy
n=2 Participants
Subjects will use the MR-010 three times a week for 30 minutes per session for 90 days. Subjects will undergo a 10-meter walk test bi-weekly and at 45 and 90 days. MR-010: MR-010 includes a patient application and sensors with commercially available headphones and smartphones. Sensors are placed on the subject's shoes and measure gait metrics. The algorithm uses data from the sensors to inform changes made to the audio cues. These cues, which are embedded in time-shifted music, are delivered back to the users who aim to walk to the beat.
Standard of Care
n=2 Participants
Subjects will undergo a 10-meter walk test bi-weekly for 90 days and at 45 and 90 days
Readmission to Hospital
0 Participants
0 Participants

Adverse Events

MR-010 Walking Therapy

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Standard of Care

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Dr. Brian Silver

UMass Chan Medical School/UMass Memorial Health

Phone: 508-334-5989

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place