A Prehabilitation Program to Boost Postoperative Functional Capacity in Surgical Lung Cancer Patients: a Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This research study is evaluating a prehabiliation intervention designed to improve postoperative functional capacity (measured by 6-minure walking distance) in individuals undergoing lung resection for cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 45
Maximum Age: 80
Healthy Volunteers: f
View:

• Patients who are diagnosed of stage I, II, or IIIA Non-small-cell lung carcinoma (NSCLC) diagnosis, with or without pre-operative histologic confirmation

• Patients scheduled to undergo lung resection surgery at least two weeks from recruitment

• Patients with a Eastern Cooperative Oncology Group (ECOG) score of 0 or 1 at recruitment

• Patients with no evidence of recurrent or progressive disease

• Patients aged 45-80 years

• Patients able to communicate in Cantonese, Mandarin, or English

• Patients is absence of any cognitive impairment

• Patients with a score of 6 minutes walking test (6MWT) ≤ 500 meters at baseline. \[rationale: a threshold value of 500 meters preoperative 6MWT predicts a higher risk of postoperative complications and prolonged LOS after lung resection\]

• Engagement in less than 150 minutes of moderate aerobic activity per week in the past 3 months

Locations
Other Locations
Hong Kong Special Administrative Region
Queen Mary Hospital
RECRUITING
Hong Kong
Contact Information
Primary
Chia-chin Lin, PhD
cclin@hku.hk
39176614
Backup
Xinyi Xu, BSN
xuxinyi@connect.hku.hk
39176948
Time Frame
Start Date: 2021-05-14
Estimated Completion Date: 2025-06-01
Participants
Target number of participants: 198
Treatments
Experimental: Prehabilitation intervention
Participants in the intervention group will follow a 2-week prehabilitation program before lung resection.
Active_comparator: Health education control
Participants in the control group will receive health education classes during 2 weeks before lung resection.
Related Therapeutic Areas
Sponsors
Leads: The University of Hong Kong

This content was sourced from clinicaltrials.gov