Pulmonary Rehabilitation in Advanced Non-small Cell Lung Cancer Patients

Sponsor
Instituto Nacional de Cancerologia de Mexico (Other)
Overall Status
Unknown status
CT.gov ID
NCT02978521
Collaborator
(none)
94
1
2
26
3.6

Study Details

Study Description

Brief Summary

Lung cancer (LC) is usually diagnosed in advanced stages and continues to be the leading cause of cancer related deaths worldwide. Cancer cachexia are frequent among patients with LC affecting up to 80% of patients with advanced stage disease, and it has been related with higher risk of complications, length of hospital stay, and worst overall survival. During cancer cachexia, both muscle and fat mass can be wasted, however, the loss of muscle mass has been associated to higher treatment related toxicity, loss of functional status, shorter progression free survival and overall survival in different types of cancer under various treatments. Hence, preservation of muscle mass and function should be an important focus of the multidisciplinary treatment of patients with LC.

Pulmonary rehabilitation (PR) has been known to improve pulmonary function, reduce fatigue and improve exercise tolerance in patients with LC undergoing curative surgery. However, few studies have focused on the efficacy of PR on patients with advanced cancer undergoing palliative care with chemotherapy or targeted therapies.

Condition or Disease Intervention/Treatment Phase
  • Other: Pulmonary rehabilitation
N/A

Detailed Description

The main objective of this study is to determine the effects of a pulmonary rehabilitation program on the pulmonary function and muscle mass. Moreover, the effects on exercise tolerance, inflammatory response, quality of live and overall survival will be explored.

Patients will be randomized into intervention group (IG) or control group (CG). Patients in the IG will be scheduled to receive 12 sessions of PR over a period of 4-6 weeks (2-3 session/week). CG will receive information and recommendations on physical activity. Both groups will receive nutritional assessment and intervention as needed.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
94 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Effect of a Pulmonary Rehabilitation Program on Skeletal Muscle Mass, Pulmonary Function, Inflammatory Response and Overall Survival on Patients Diagnosed With Non-small-cell Advanced Cancer
Study Start Date :
Aug 1, 2016
Anticipated Primary Completion Date :
Aug 1, 2018
Anticipated Study Completion Date :
Oct 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group

Patients in the IG will be scheduled to receive Pulmonary Rehabilitation: 12 sessions (60 minutes approximately) over a period of 4-6 weeks (2-3 session/week). Sessions will progress as patients tolerance to exercise and will include breathing techniques, resistance training on ergometer and treadmill.

Other: Pulmonary rehabilitation
Session 1: ventilatory pattern training Session 2,3: ventilatory pattern + respiratory training with incentive spirometer Session 4-6: Sessions 1-3 training continues + training with Positive expiratory pressure device (Threshold PEP) and breathing trainer Threshold IMT) Sessions 7-9: Continue respiratory training + resistance training with RECK MOTOmed2 ergometer at a 30% intensity until 60% is achieved Session 10-12: Continue with previous training + treadmill training

No Intervention: Control Group

CG will receive information and recommendations on physical activity

Outcome Measures

Primary Outcome Measures

  1. Pulmonary function [After 12 sessions (6 weeks)]

    Pulmonary function Maximal expiratory and inspiratory pressure units: cm H2O (measured with Jaeger spirometer)

Secondary Outcome Measures

  1. Muscle mass [After 12 sessions (6 weeks)]

    Muscle mass measured by body composition analysis of CT images using lumbar vertebra 3 (L3)

  2. Inflammatory response [After 12 sessions (6 weeks)]

    Quantification of: Interleukin (IL)-8, IL-1β, IL-6, IL-10, IL-12 and tumor necrosis factor (TNF) (Human Inflammatory Cytokine Kit Becton, Dickinson and Company (BD)™ Cytometric Bead Array) Units: pg/ml

  3. Exercise tolerance [After 12 sessions (6 weeks)]

    6 minute walk test

  4. Quality of Life [After 12 sessions (6 weeks)]

    Application of the "european organization for research and treatment of cancer quality of life questionnaire (QLQ)-C30

  5. Lung Cancer Quality of Life [After 12 sessions (6 weeks)]

    Application of the "european organization for research and treatment of cancer quality of life questionnaire (QLQ)LC-13"

  6. Anxiety and Depression [After 12 sessions (6 weeks)]

    Hospital Anxiety and Depression Scale (HADS

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Confirmed diagnosis of advanced non-small-cell lung cancer

  • Good performance status (ECOG 0-1)

  • Life expectancy >12 weeks

  • Eligible to receive treatment with chemotherapy or tyrosinkinase inhibitors

  • Recent electrocardiogram without evidence of arrythmia

Exclusion Criteria:
  • Symptomatic brain metastasis

  • Uncontrolled pain (Visual Analog Scale >5)

  • Uncontrolled hypertension (>140/100mmHg)

  • Practice of regular moderate to intense physical activity at least 3 day/week

  • Not residents of Mexico City or unable to attend to therapy sessions

Contacts and Locations

Locations

Site City State Country Postal Code
1 Instituto Nacional de Cancerología Mexico Distrito Federal Mexico 14080

Sponsors and Collaborators

  • Instituto Nacional de Cancerologia de Mexico

Investigators

  • Study Director: Oscar Arrieta, Head of Thoracic Oncology Unit

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Oscar Gerardo Arrieta Rodríguez MD, Principal Investigator, Head of the Thoracic Oncology Unit, Instituto Nacional de Cancerologia de Mexico
ClinicalTrials.gov Identifier:
NCT02978521
Other Study ID Numbers:
  • 016/028/ICI
First Posted:
Dec 1, 2016
Last Update Posted:
Dec 1, 2016
Last Verified:
Nov 1, 2016
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 1, 2016