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Spots Global Cancer Trial Database for Perioperative Rehabilitation in Operation for Lung Cancer

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Trial Identification

Brief Title: Perioperative Rehabilitation in Operation for Lung Cancer

Official Title: Perioperative Rehabilitation in Operation for Lung Cancer

Study ID: NCT01893580

Study Description

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.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Copenhagen Centre for Cancer and Health, Copenhagen, Nørrebro, Denmark

Contact Details

Name: Jesper Holst Pedersen, MD, DrMSci

Affiliation: Department of Cardiothoracic Surgery RT

Role: STUDY_CHAIR

Name: Jette Vibe-Petersen, MD

Affiliation: Copenhagen Centre for Cancer and Health

Role: STUDY_DIRECTOR

Name: Maja Schick Sommer, MHS

Affiliation: Copenhagen Centre for Cancer and Health

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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