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Multimodal Intervention for Patients With Non-small Cell Lung Cancer

Primary Purpose

Cachexia; Cancer

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
multimodal
Sponsored by
Aalborg University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cachexia; Cancer focused on measuring cachexia, cancer, multimodal intervention

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • histopathologically or cytologically verified with NSCLC
  • inoperable tumour, candidates for, but naïve to or no systemic anti-neoplastic treatment the previous two years
  • commence first line of chemotherapy (carboplatin/vinorelbin, cisplatin/vinorelbin) with or without radiation therapy or pembrolizumab
  • performance status ≤2 (Eastern Cooperative Oncology Group)
  • age >18 and provided oral
  • written consent

Exclusion Criteria:

  • excessive alcohol or drug abuse
  • incapable to follow the intervention (i.e. cognitive problems or unable to walk) were excluded.

Sites / Locations

  • Aalborg Univeristy Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention group

Historical control group

Arm Description

2 g EPA/DHA via fish oil daily Regular dietary counselling Twice weekly strength and cardiovascular exercise

Standard of Care

Outcomes

Primary Outcome Measures

Feasibility, recruitment rate
Recruitment rate is measured by dividing the number of patients consented by the number of patients screened
Feasibility, retention rate
Retention rate is measured by dividing the number of patients completing the trial with the number of patients consented
Feasibility, compliance
The overall compliance was defined successful if at least half of the included patients reached at least 75 % of the nutrient target, consumed at least 75 % of the fish oil and conducted at least 50 % of the physical exercises

Secondary Outcome Measures

Predictive and prognostic factors of change in skeletal muscle
Change in skeletal muscle was measured using CT scans, analysed at the 3rd lumbar vertebra, expressed as actual change in square centimeter. Using an ordinal logistic regression model, patients were ordered in three Groups (muscle wasting: loss of at least 6 cm^2 ; muscle maintenance: +/- 5.9 cm^2; muscle gain: gain of at least 6.0 cm^2). The baseline variables included in the model are age, gender, tumor stage, type of treatment, performance status, inflammatory score (mGPS) and cachexia. The possible prognostic factors included in the model is change in body weight, adherence to the anti-neoplastic treatment plan, treatment response, compliance to the multimodal intervention, number of Nutrition impact symptoms, days in between CT scans, energy and protein intake.
Group difference in body weight
The change in body weight (measured at baseline and at the end of the trial using body weight scales, expressed as %
Group difference in skeletal muscle
Change in skeletal muscle (measured using CT scans, expressed as actual muscle change at the 3rd lumbar vertebra in mean (SD) cm^2
Proportion of patients gaining, maintaining and wasting of skeletal muscle
expressed as number of patients. Gaining defined as at least +6 Square centimeter skeletal muscle. Maintaining defined as: +/- 5.9 Square centimeter skeletal muscle. Wasting defined as: at least -6 Square centimeter skeletal muscle
Change in physical function
assessed by timed-up-and-go test (expressed in number of seconds) and assessed by 30 seconds sit-to-stand test (expressed as number of stands).

Full Information

First Posted
September 24, 2019
Last Updated
November 11, 2019
Sponsor
Aalborg University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04161794
Brief Title
Multimodal Intervention for Patients With Non-small Cell Lung Cancer
Official Title
Multimodal Intervention (Dietary Counselling, Fish Oil and Physical Training) for Patients With Non-small Cell Lung Cancer, a Feasibility Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
February 15, 2018 (Actual)
Primary Completion Date
April 30, 2019 (Actual)
Study Completion Date
April 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aalborg University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
A single-arm intervention study assessing the feasibility of a multimodal intervention of management of cancer cachexia in patients with non-small cell lung cancer during primary anti-neoplastic treatment. The effects of the intervention is compared to a historical control group
Detailed Description
In a single arm intervention study, we will provide a multimodal intervention consisting of dietary counselling, physical exercises plan as well as fish oil. The target of the dietary counselling is: 30 kcal/kg/d (in patients with BMI <30) or 25 kcal/kg/d (in patients with BMI => 30) at least 1.0 g protein/kg/d three daily meals of at least 20 g of protein restrict overnight fasting to a maximum of 11 hours The initial dietary counselling is at the first cycle of anti-neoplastic treatment. The patient will be provided an individual plan to meet the dietary targets tailored to the individual preferences and symptoms. At every cycle of anti-neoplastic treatment, the plan will be adjusted if needed. At every week the patients will be prompted by telephone to comply with the dietary plan. The physical exercise consists of two exercises: strength training: a progressive sit-to-stand exercise which is a lower extremity exercise. cardio-vascular training: a progressive brisk walking plan. Patients are prompted to execute both exercises twice weekly. The individual targets are set at the first cycle of anti-neoplastic treatment and adjusted during the trial. Fish oil: The patients are instructed to ingest 10g of liquid fish oil (consisting of 2 g EPA/DHA) or 8 capsules of fish oil (consisting of 2 g EPA/DHA)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cachexia; Cancer
Keywords
cachexia, cancer, multimodal intervention

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
This is a single arm intervention study, comparing the results to that of a historical control Group.
Masking
None (Open Label)
Masking Description
Non-randomised
Allocation
Non-Randomized
Enrollment
58 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
2 g EPA/DHA via fish oil daily Regular dietary counselling Twice weekly strength and cardiovascular exercise
Arm Title
Historical control group
Arm Type
No Intervention
Arm Description
Standard of Care
Intervention Type
Other
Intervention Name(s)
multimodal
Intervention Description
2 g EPA/DHA as fish oil, repeated dietary counselling and twice weekly 2 x exercises
Primary Outcome Measure Information:
Title
Feasibility, recruitment rate
Description
Recruitment rate is measured by dividing the number of patients consented by the number of patients screened
Time Frame
9 months
Title
Feasibility, retention rate
Description
Retention rate is measured by dividing the number of patients completing the trial with the number of patients consented
Time Frame
9 months
Title
Feasibility, compliance
Description
The overall compliance was defined successful if at least half of the included patients reached at least 75 % of the nutrient target, consumed at least 75 % of the fish oil and conducted at least 50 % of the physical exercises
Time Frame
9-18 weeks
Secondary Outcome Measure Information:
Title
Predictive and prognostic factors of change in skeletal muscle
Description
Change in skeletal muscle was measured using CT scans, analysed at the 3rd lumbar vertebra, expressed as actual change in square centimeter. Using an ordinal logistic regression model, patients were ordered in three Groups (muscle wasting: loss of at least 6 cm^2 ; muscle maintenance: +/- 5.9 cm^2; muscle gain: gain of at least 6.0 cm^2). The baseline variables included in the model are age, gender, tumor stage, type of treatment, performance status, inflammatory score (mGPS) and cachexia. The possible prognostic factors included in the model is change in body weight, adherence to the anti-neoplastic treatment plan, treatment response, compliance to the multimodal intervention, number of Nutrition impact symptoms, days in between CT scans, energy and protein intake.
Time Frame
9-18 weeks
Title
Group difference in body weight
Description
The change in body weight (measured at baseline and at the end of the trial using body weight scales, expressed as %
Time Frame
9-18 weeks
Title
Group difference in skeletal muscle
Description
Change in skeletal muscle (measured using CT scans, expressed as actual muscle change at the 3rd lumbar vertebra in mean (SD) cm^2
Time Frame
9-18 weeks
Title
Proportion of patients gaining, maintaining and wasting of skeletal muscle
Description
expressed as number of patients. Gaining defined as at least +6 Square centimeter skeletal muscle. Maintaining defined as: +/- 5.9 Square centimeter skeletal muscle. Wasting defined as: at least -6 Square centimeter skeletal muscle
Time Frame
9-18 weeks
Title
Change in physical function
Description
assessed by timed-up-and-go test (expressed in number of seconds) and assessed by 30 seconds sit-to-stand test (expressed as number of stands).
Time Frame
9-18 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: histopathologically or cytologically verified with NSCLC inoperable tumour, candidates for, but naïve to or no systemic anti-neoplastic treatment the previous two years commence first line of chemotherapy (carboplatin/vinorelbin, cisplatin/vinorelbin) with or without radiation therapy or pembrolizumab performance status ≤2 (Eastern Cooperative Oncology Group) age >18 and provided oral written consent Exclusion Criteria: excessive alcohol or drug abuse incapable to follow the intervention (i.e. cognitive problems or unable to walk) were excluded.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mette Holst, PhD
Organizational Affiliation
Aalborg University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Aalborg Univeristy Hospital
City
Aalborg
ZIP/Postal Code
9000
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32600857
Citation
Tobberup R, Carus A, Rasmussen HH, Falkmer UG, Jorgensen MG, Schmidt EB, Jensen NA, Mark EB, Delekta AM, Antoniussen CS, Bogsted M, Holst M. Feasibility of a multimodal intervention on malnutrition in patients with lung cancer during primary anti-neoplastic treatment. Clin Nutr. 2021 Feb;40(2):525-533. doi: 10.1016/j.clnu.2020.05.050. Epub 2020 Jun 9.
Results Reference
derived

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Multimodal Intervention for Patients With Non-small Cell Lung Cancer

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