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Evaluation of the Effect of Remote Assistance by A Nurse To Preoperative Respiratory Rehabilitation in Video-assisted Thoracic Surgery Lobectomy or Segmentectomy: A randomized controlled trial

Evaluation of the Effect of Remote Assistance by A Nurse To Preoperative Respiratory Rehabilitation in Video-assisted Thoracic Surgery Lobectomy or Segmentectomy: A randomized controlled trial - Evaluation of the Effect of Remote Assistance by A Nurse To Preoperative Respiratory Rehabilitation in Video-assisted Thoracic Surgery Lobectomy or Segmentectomy: A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000047075
Enrollment
50
Registered
2022-03-04
Start date
2022-03-05
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

malignant lung tumor

Interventions

For breathing training at home during the hospitalization waiting period Intervention group: performed with remote assistance from nurses / Control group: performed by themselves without nurse assist

Sponsors

NTT Medical Center Tokyo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients with malignant tumors who meet the indication criteria of the critical path for thoracoscopic lobectomy Criteria for indication for thoracoscopic lobectomy path at cooperating institutions: cases in which specoscopic lobectomy and sectional resection are performed. (2) Those who have a smart phone, computer or phone (3) Patients who can perform preoperative respiratory rehabilitation by themselves at home. (4) Those who have been fully informed and have given their free and voluntary written consent to participate in this study.

Exclusion criteria

Exclusion criteria: (1) Patients with malignant tumors undergoing procedures other than thoracoscopic lobectomy and segmentectomy (2) Those whose attending physician predicts that the patient will not progress according to the thoracoscopic lobectomy critical path after the operation based on the patient's condition. (3) Patients who have physical or mental difficulties in performing preoperative respiratory rehabilitation. (4) Those who cannot give consent to participate in this study. (5) Persons who are judged by the attending physician, principal investigator, or principal study authorization holder to be inappropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
Number of postoperative days in the hospital

Countries

Japan

Contacts

Public ContactYasuko Muraki

Tokai University Graduate School Medicine Course

0cmud013@cc.u-tokai.ac.jp0463-93-1121

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026