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Rehabilitation for Thoracoscopic Lobectomy

NCT04502654 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 32

Last updated 2021-08-16

No results posted yet for this study

Summary

The main aim of this research is to compare the functional recovery after discharge with the preoperative physical activity as a hypothesis generating study.

Conditions

  • Lung Neoplasms
  • Rehabilitation
  • Exercise
  • Pain, Postoperative
  • Post Discharge

Interventions

DEVICE

Actiwatch 2 (Philips Respironics, Murrysville, USA)

Actiwatch 2 is an unobtrusive, waterproof, light sensor and wrist-worn device (weight 16.0g, size 4.3 cm\* 2.3 cm\* 1.0 cm), containing a tri-axial accelerometer able to records a digitally integrated measure of gross motor activity (a piezoelectric sensor to detect vertical accelerations at the wrist between 0.5 and 2.0 g with a frequency response range between 0.35-7.5 Hz). Activity counts from the device reflect the peak acceleration detected over each epoch and are used in determining sleep and wake intervals, which can be used to rest-activity patterns, quality of physical activity and sleep for 15-60 seconds/ epoch, 24 hours/ day, 2 weeks.

Sponsors & Collaborators

  • Rigshospitalet, Denmark

    lead OTHER

Principal Investigators

  • Lin Huang, MD · Rigshospitalet, Denmark

  • Henrik Kehlet, Professor, MD, DMSc · Rigshospitalet, Denmark

  • Rene H Petersen, Professor, MD, PhD · Rigshospitalet, Denmark

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-15
Primary Completion
2021-07-21
Completion
2021-07-21

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04502654 on ClinicalTrials.gov