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Effect of Prehabilitation Protocol on Quality of Life After Thoracoscopic Surgery (VATS)

A

Assiut University

Status

Completed

Conditions

Thoracoscopy
Prehabilitation

Treatments

Other: Educational nursing protocol
Other: Routine hospital care

Study type

Interventional

Funder types

Other

Identifiers

NCT03915093
1562017

Details and patient eligibility

About

video-assisted thoracic surgery (VATS) is a new approach used in cardio thoracic surgery department instead of thoracotomy to treat several diseases.patients underwent thoracoscopic surgery without organized educational protocol either before or after the procedure. Therefore, this study will be the first clinical research which will increase patients' knowledge about thoracoscopy and decrease its complications.

Full description

The role of thoracic nursing specialty is to support and educate patients, who are suffering from thoracic diseases, to achieve the best outcome in terms of physical, psychological, social and spiritual well beings. The care provided not only focuses on in-hospital treatments that patient received, but also encompasses the whole patient journey including lifestyle modification, health concept promotion, self-empowerment and secondary prevention. Preoperative prophylactic physiotherapy has been shown to be an important and effective approach in preventing or reducing postoperative complications, in addition to optimizing treatment by familiarizing the patient with the physiotherapeutic procedures. Quasi experimental research design was utilized to conduct this study.Sixty adult patients undergoing thoracoscopic surgery included and had the following criteria, the age ranged from 18-65 years old, both male and female. The patients divided into two equal groups (study and control groups), 30 patients for each. The study group received educational nursing protocol while the control group received the routine hospital care.

Enrollment

60 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who undergoing thoracoscopic surgery
  • Age 18-65 year
  • patients who agree to participate in the study

Exclusion criteria

  • converting to thoracotomy
  • patients refuse to participate

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

study group
Experimental group
Description:
receive educational nursing protocol
Treatment:
Other: Routine hospital care
Other: Educational nursing protocol
control group
Active Comparator group
Description:
receive routine hospital care
Treatment:
Other: Routine hospital care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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