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Perioperative Rehabilitation in Operation for Lung Cancer

Perioperative Rehabilitation in Operation for Lung Cancer

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01893580
Acronym
PROLUCA
Enrollment
40
Registered
2013-07-09
Start date
2012-05-31
Completion date
2015-01-31
Last updated
2015-05-07

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

Conditions

Lung Cancer, Non Small Cell Lung Cancer

Keywords

Cancer, Rehabilitation, Exercise, Lung cancer, NSCLC

Brief summary

Background: Improved surgical techniques combined with effective adjuvant chemotherapy, has led to a better survival in individuals with NSCLC. The treatment of NSCLC and other cancer diseases are after all still complex and potentially lethal. Study aim: The rationale for the study PROLUCA is to identify the optimal timing of exercise to improve recovery after surgery in patients operated for lunge cancer with focus on physical capacity and quality of life. Who can participate? Patients above 18 years and diagnosed with lung cancer and referred for operation. Participation in this study is not possible if the participants by a doctor are advised not to do strenuous exercise. What does the study involve? The intervention consists of a combination of (1) exercise before surgery and (2) exercise after surgery for lung cancer. 1. Exercise before surgery is a home-based exercise program is individually designed and must be performed for at least 30 minutes every day until surgery. The home-based exercise program varies in length due to number of days until surgery, and the intention is not exceed 14 days. 2. The exercise initiated two weeks and 6 weeks after surgery consists of a 12 weeks rehabilitation program and three individual counseling sessions. Special needs in terms of smoking cessation, nutritional counseling or patient education, this is also offered. The exercise consists of individually prepared supervised strength - and fitness exercise in a team, two sessions of 60 minutes/week. What interventions will be compared? A home-based post-operative exercise program, combined with exercise initiated two weeks after surgery, will be compared with usual care (exercise initiated six weeks after surgery). Will all participants receive the same treatment? By draw it is decided which of the 4 groups the participants will attend to in the study: * Group 1: Home-based exercise before surgery and rehabilitation initiated as early as two weeks after surgery * Group 2: Home-based exercise before surgery and rehabilitation initiated six weeks after surgery * Group 3: Rehabilitation initiated as early as two weeks after surgery * Group 4: Rehabilitation initiated six weeks after surgery (Usual practice as control group) What are the possible benefits and risks of participating? There are no risks or side- effects of participating other than muscle soreness and exercise is beneficial when it comes to recover from an operation from lung cancer.

Interventions

BEHAVIORALExperimental: 1. Experimental

Home-based exercise pre surgery and postoperative exercise in a team initiated two weeks after surgery. Intervention consists of: 1. Preoperative home-based exercise program - cardiovascular exercise of moderate-vigorous intensity for at least 30 minutes every day until surgery. 2. Postoperative rehabilitation: A supervised 12-week rehabilitation program containing 24 group-based exercise sessions, three individual counseling sessions and smoking cessation, nutritional counseling or patient education, this is offered too.The cardiorespiratory intensity is at \ 50-60% of individual HRmax for the first four weeks and increases to moderate-high intensity at \ 70-90% of individually determined HRmax. The intensity of the strength exercise program is at \ 60-80% of 1 RM.

BEHAVIORALExperimental: 2. Experimental

Home-based exercise pre surgery and postoperative exercise in a team initiated six weeks after surgery. Intervention consists of: 1. Preoperative home-based exercise program - cardiovascular exercise of moderate-vigorous intensity for at least 30 minutes every day until surgery. 2. Postoperative rehabilitation: A supervised 12-week rehabilitation program containing 24 group-based exercise sessions, three individual counseling sessions and smoking cessation, nutritional counseling or patient education, this is offered too.The cardiorespiratory intensity is at \ 50-60% of individual HRmax for the first four weeks and increases to moderate-high intensity at \ 70-90% of individually determined HRmax. The intensity of the strength exercise program is at \ 60-80% of 1 RM.

BEHAVIORALExperimental: 3. Experimental

Early postoperative exercise in a team initiated two weeks after surgery. Intervention consists of: Postoperative rehabilitation: A supervised 12-week rehabilitation program containing 24 group-based exercise sessions, three individual counseling sessions and smoking cessation, nutritional counseling or patient education, this is offered too.The cardiorespiratory intensity is at \ 50-60% of individual HRmax for the first four weeks and increases to moderate-high intensity at \ 70-90% of individually determined HRmax. The intensity of the strength exercise program is at \ 60-80% of 1 RM.

BEHAVIORALOther: 4. Usual care

Exercise in a team initiated six weeks after surgery consisting of a supervised 12-week rehabilitation program containing 24 group-based exercise sessions, three individual counseling sessions, and three group-based lessons in health-promoting behavior. If the participants have special needs in terms of smoking cessation, nutritional counseling or patient education, this is offered too. The cardiorespiratory intensity is at \ 50-60% of individual HRmax for the first four weeks. The next eight weeks the intensity increases to moderate-high intensity at \ 70-90% of individually determined HRmax. The intensity of the strength exercise program is at \ 60-80% of 1 RM.

Sponsors

Centre for Integrated Rehabilitation of Cancer patients, CIRE, Denmark
CollaboratorUNKNOWN
Danish Cancer Society
CollaboratorOTHER
Novo Nordisk A/S
CollaboratorINDUSTRY
University of Copenhagen
CollaboratorOTHER
Copenhagen Centre for Cancer and Health, Denmark.
CollaboratorUNKNOWN
Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Performance status 0-2 (WHO) * Living in the City of Copenhagen or surrounding Municipalities * Ability to read and understand Danish * Approval by primary surgeon

Exclusion criteria

* Presence of metastatic disease or surgical inoperability * Diagnosis of Lung Cancer not verified by histological diagnosis * Cardiac disease

Design outcomes

Primary

MeasureTime frameDescription
Maximum oxygen uptake (VO2peak)VO2peak is assessed at baseline, the day before surgery, post-intervention (14/18 weeks after surgery), six months after surgery, and one year after surgery.VO2peak is evaluated by an incremental test using an electromagnetically braked cycle ergometer (Lode Corival Ergometer©). Inspired and expired gases are analyzed breath-by-breath by a metabolic cart (JAEGER MasterScreen CPX©). Subjects begin pedaling at seven watts and resistance increases after a predefined 10 watts ramp protocol until exhaustion or a symptom-limited VO2peak is achieved (pain, dizziness, anxiety etc.).

Secondary

MeasureTime frameDescription
Six minute walk distance (6MWD)baseline, the day before surgery, pre-intervention (2/6 weeks after surgery), post-intervention (14/18 weeks after surgery), six months after surgery, and one year after surgery.
Patient reported outcomes (PROs)Baseline, the day before surgery, pre-intervention (2/6 weeks after surgery), post-intervention (14/18 weeks after surgery), six months after surgery, and one year after surgery.PROs will include health related quality of life, symptoms and side-effects, anxiety and depression, well-being, distress, lifestyle, sickness absence, work status, and social support.
Pulmonary functionBaseline, the day before surgery, post-intervention (14/18 weeks after surgery), six months after surgery, and one year after surgery.forced expiratory volume at one second

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026