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Rehabilitation for Thoracoscopic Lobectomy

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Rigshospitalet

Status

Completed

Conditions

Lung Neoplasms
Rehabilitation
Post Discharge
Pain, Postoperative
Exercise

Treatments

Device: Actiwatch 2 (Philips Respironics, Murrysville, USA)

Study type

Observational

Funder types

Other

Identifiers

NCT04502654
H-20041489

Details and patient eligibility

About

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

Enrollment

32 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • VATS-L
  • Speaks and understands Danish or English.
  • Informed consent obtained

Exclusion criteria

  • Co-VATS-L.
  • on the wheelchair.
  • Living in nurse home.
  • Using rollator to assist to walk.
  • Unwilling to place the Actiwatch 2 or execute PPE.

Trial design

32 participants in 1 patient group

Pilot group
Description:
As a pilot Group for observating variable rehabilitation under individual baselines.
Treatment:
Device: Actiwatch 2 (Philips Respironics, Murrysville, USA)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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