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Effects of Protein on Muscle, Gut Microbiota and Clinical Outcome in Patients With Lung Cancer-related Sarcopenia

Primary Purpose

Lung Cancer, Sarcopenia

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
soy protein
whey protein
placebo
Sponsored by
Peking Union Medical College Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lung Cancer focused on measuring soy protein, whey protein, lung cancer related sarcopenia

Eligibility Criteria

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

Inclusion Criteria: age>=18years old Patients with lung cancer and sarcopenia ECOG<=2 Patients are able to provide written informed consent. Exclusion Criteria: People who are allergic to soy protein and whey protein. Participants received any drugs or supplements known to influence effcet size, such as protein powder, anabolic steroids, or glucorticosteroid before the 3 months preceding the study. Participants with gastrointestinal bleeding, enterotomy or gastric bypass surgery before the 3 months preceding the study. Concurrent severe cardiac disease, liver and renal failure, which may significantly interfere with study compliance. Participants with electronic or mental device.

Sites / Locations

  • Peking Union Medical College Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

soy protein intervention

whey protein intervention

control

Arm Description

This group received dietary guidance and soy protein intervention for 3 months

This group received dietary guidance and whey protein intervention for 3 months

This group received dietary guidance and mltodextrin for 3 months

Outcomes

Primary Outcome Measures

Change from Baseline Appendicular skeletal muscle mass index at 3 months
Defined as muscle mass (Unit: kg/m2)

Secondary Outcome Measures

Change from Baseline Hand grip at 3 months
Defined as muscle strength (Unit: kg)
Change from Baseline physical performance Baseline at 3 months
Measured by Short Physical Performance Battery (0-12) with higher scores meaning better physical performance.
Change from Baseline Physical function at 3 months
Measured by FRAIL scale (0-5) with higher scores meaning better physical function.
Change from Baseline Quality of life questionnaire at 3 months
Measured by EuroQol- 5 Dimension scale (0-5) with higher scores meaning better Quality of life.
Change from Baseline gut microbiota composition at 3 months
The stool samples of participants before and after intervention were collected and analized by 16S rRNA.
Number of patients with good Chemotherapy Tolerance
Completing initially planned chemotherapy course is defined as good tolerance; dose adjustment, delayed completion or interruption of treatment are considered as poor tolerance.
Incidence of Chemotherapy toxicity
Measured after initiation of chemotherapy using the WHO Toxicity Grades (gradeI-IV) with higher grades neaning severer chemotheraphy toxicity.

Full Information

First Posted
February 23, 2023
Last Updated
March 5, 2023
Sponsor
Peking Union Medical College Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05771207
Brief Title
Effects of Protein on Muscle, Gut Microbiota and Clinical Outcome in Patients With Lung Cancer-related Sarcopenia
Official Title
Effects of Soy Protein and Whey Protein on Muscle, Gut Microbiota and Clinical Outcome in Patients With Lung Cancer-related Sarcopenia(LCRS): a Randomized, Double-blind, Controlled Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 2023 (Anticipated)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
January 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking Union Medical College Hospital

4. Oversight

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

5. Study Description

Brief Summary
Sarcopenia is common in lung cancer patients. It is one of the significant factors affecting the overall survival, radiotherapy and chemotherapy efficacy, and quality of life of patients with lung cancer. Previous studies have shown that increased protein intake can stimulate postprandial muscle synthesis, and improve muscle mass, strength, function, and overall survival. However, most previous studies have focused on the intervention of whey protein, while the protective effect of soybean protein on lung cancer-related sarcopenia (LCRS) has not yet been fully explored and reached an agreement. So, this study aims to explore the effects of soy and whey protein on muscle, gut microbiota, and clinical outcomes among patients with lung cancer-related sarcopenia, to provide a reference for further nutrition treatment.
Detailed Description
This study will last 6 months. For the duration of the study, an anticipated total of 90 participants will be randomly assigned to receive either a 30-gram protein supplement or a placebo daily. There will be a total of 5 study visits, and dietary records, questionnaires, blood and stool collection, and functional testing will occur at all study visits. Intention-to-treat analysis (ITT) and per-protocol analysis (PP) will be conducted in statistical analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer, Sarcopenia
Keywords
soy protein, whey protein, lung cancer related sarcopenia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
soy protein intervention
Arm Type
Experimental
Arm Description
This group received dietary guidance and soy protein intervention for 3 months
Arm Title
whey protein intervention
Arm Type
Experimental
Arm Description
This group received dietary guidance and whey protein intervention for 3 months
Arm Title
control
Arm Type
Placebo Comparator
Arm Description
This group received dietary guidance and mltodextrin for 3 months
Intervention Type
Dietary Supplement
Intervention Name(s)
soy protein
Intervention Description
The intervention is made up of soy protein supplements (30g/d) and dietary pattern modification.
Intervention Type
Dietary Supplement
Intervention Name(s)
whey protein
Intervention Description
The intervention is made up of whey protein supplements (30g/d) and dietary pattern modification.
Intervention Type
Dietary Supplement
Intervention Name(s)
placebo
Intervention Description
The intervention is made up of maltodextrin (30g/d) and dietary pattern modification.
Primary Outcome Measure Information:
Title
Change from Baseline Appendicular skeletal muscle mass index at 3 months
Description
Defined as muscle mass (Unit: kg/m2)
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Change from Baseline Hand grip at 3 months
Description
Defined as muscle strength (Unit: kg)
Time Frame
3 months
Title
Change from Baseline physical performance Baseline at 3 months
Description
Measured by Short Physical Performance Battery (0-12) with higher scores meaning better physical performance.
Time Frame
3 months
Title
Change from Baseline Physical function at 3 months
Description
Measured by FRAIL scale (0-5) with higher scores meaning better physical function.
Time Frame
3 months
Title
Change from Baseline Quality of life questionnaire at 3 months
Description
Measured by EuroQol- 5 Dimension scale (0-5) with higher scores meaning better Quality of life.
Time Frame
3 months
Title
Change from Baseline gut microbiota composition at 3 months
Description
The stool samples of participants before and after intervention were collected and analized by 16S rRNA.
Time Frame
3 months
Title
Number of patients with good Chemotherapy Tolerance
Description
Completing initially planned chemotherapy course is defined as good tolerance; dose adjustment, delayed completion or interruption of treatment are considered as poor tolerance.
Time Frame
3 months
Title
Incidence of Chemotherapy toxicity
Description
Measured after initiation of chemotherapy using the WHO Toxicity Grades (gradeI-IV) with higher grades neaning severer chemotheraphy toxicity.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age>=18years old Patients with lung cancer and sarcopenia ECOG<=2 Patients are able to provide written informed consent. Exclusion Criteria: People who are allergic to soy protein and whey protein. Participants received any drugs or supplements known to influence effcet size, such as protein powder, anabolic steroids, or glucorticosteroid before the 3 months preceding the study. Participants with gastrointestinal bleeding, enterotomy or gastric bypass surgery before the 3 months preceding the study. Concurrent severe cardiac disease, liver and renal failure, which may significantly interfere with study compliance. Participants with electronic or mental device.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kang Yu, MD
Phone
+8613801130457
Email
yuk1997@sina.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yu Zang, MD
Phone
+8617332739749
Email
zhangyu_a0849@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kang Yu, MD
Organizational Affiliation
Peking Union Medical College Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking Union Medical College Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100730
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

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Effects of Protein on Muscle, Gut Microbiota and Clinical Outcome in Patients With Lung Cancer-related Sarcopenia

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