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Home Rehabilitation After Acute Pulmonary Embolism

Home Rehabilitation After Acute Pulmonary Embolism

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05571189
Enrollment
32
Registered
2022-10-07
Start date
2022-12-19
Completion date
2025-09-24
Last updated
2025-10-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Embolism

Brief summary

The purpose of this study is to evaluate whether a home rehabilitation program after hospitalization for acute pulmonary embolism (PE) improves clinical outcomes at 3 months compared to usual care. Daily physical activity tasks that incorporate heart rate monitoring will be sent through email or text. This information could help improve the management of acute PE.

Interventions

BEHAVIORALDaily Activity Text

Participants will receive a text each day with instructions about the daily activity they should complete for that day.

BEHAVIORALControl Text

Participants will receive a text each day with no instructions about daily activity. It will have messages like have a nice day.

Sponsors

American College of Chest Physicians
CollaboratorOTHER
University of Rochester
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* English speaking (\>18 years old). Daily messages will be sent in English. * Acute PE with right ventricular enlargement or dysfunction defined by echocardiogram report, CT Angiogram report, or elevated cardiac biomarker (NT-pro BNP or troponin). * Baseline testing started within 7 days of hospital discharge.

Exclusion criteria

* Pregnancy. * Cardiac Effort \>2.5 beats/m during 6MWT. This is for safety. * Cardiac Effort \<1.2 beats/m during 6MWT. They are unlikely to benefit. * Resting tachycardia \>120 beats/m during screening or at hospital discharge. * Suspicion for Chronic Thromboembolic Pulmonary Hypertension. * Systolic blood pressure \>180 mmHg during screening or at hospital discharge. * Inability to walk. * Estimated prognosis \<12 months at the time of discharge due to underlying co-morbidities. * Advanced neurologic disease. * Lack of access to email or text messaging. * Inability to follow daily instructions. * Participation in a structured exercise routine at least three days per week in the prior four weeks. * Principal Investigator discretion

Design outcomes

Primary

MeasureTime frameDescription
mean change in vector magnitude count as measured by actigraphy10 weeksThe Actigraph triaxial accelerometer will be used to monitor continuous activity at home on the non-dominant wrist. The accelerometer data will be downloaded and will include the vector magnitude count.
mean change in mean amplitude deviation as measured by actigraphy10 weeksThe Actigraph triaxial accelerometer will be used to monitor continuous activity at home on the non-dominant wrist. The accelerometer data will be downloaded and will include the mean amplitude deviation.

Secondary

MeasureTime frameDescription
mean change in activity as measured by Actigraph12 weeksThe Actigraph triaxial accelerometer will be used to monitor the amount of activity taken at home on the non-dominant wrist. The accelerometer data will be downloaded and will include the amount of activity.
mean change in quality of life as measured by PROMIS12 weeksThe PROMIS questionnaire ranges from 0-99 with higher scores indicating worse outcome.
mean change in quality of life as measured by Emphasis 1012 weeksThe Emphasis 10 questionnaire ranges from 0-50 with higher scores indicating worse quality of life.
mean change in quality of life as measured by Pulmonary Embolism quality of life questionnaire12 weeksThe pulmonary embolism quality of life questionnaire ranges from 1 to 27 with higher scores indicating worse outcomes.
proportion of participants with post-PE syndrome12 weeksParticipants will be evaluated by a physician to determine if they have post PE-syndrome
mean change in heart rate during a 6 minute walk12 weeks
mean change in oxygen use during a 6 minute walk12 weeksOxygen use will be measured by a measured by portable K5 metabolic analyzer.
mean change in carbon dioxide production during a 6 minute walk12 weeksCarbon Dioxide use will be measured by a measured by portable K5 metabolic analyzer.
proportion or subjects who develop chronic thromboembolic pulmonary hypertension12 weeks
mean change in 6 minute walking distance12 weeks
mean change in steps as measured by Actigraph12 weeksThe Actigraph triaxial accelerometer will be used to monitor the number of steps taken at home on the non-dominant wrist. The accelerometer data will be downloaded and will include the step count.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026