Biomarker Identification and Nutritional Intervention of Primary Sarcopenia Based on Gut-muscle Axis
NCT ID: NCT06347835
Last Updated: 2024-04-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
120 participants
INTERVENTIONAL
2024-04-30
2026-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Improvement of Skeletal and Muscle Health in Patients With Sarcopenia by Protein Powder With Resistance Exercise
NCT07049731
Intervention Assessing the Role of Exercise Program and Nutrition Supplement for Sarcopenia
NCT02374268
Prevalence and Effect of Lifestyle Modification on Clinical Outcomes and Cost-effectiveness Ratio for Sarcopenia
NCT02873676
The Effect of a Multi-intervention Program and Protein Food Sources on Preventing and Mitigating Sarcopenia
NCT06173271
Protein and Skeletal Muscle in Older Twins: Role of the Gut Microbiome
NCT04309292
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
symbiotic and whey protein intervention
This group received dietary guidance, symbiotic and whey protein intervention for 12 weeks
symbiotic
The intervention is made up of multiple probiotics and prebiotics (20g/d) and dietary pattern modification.
whey protein
The intervention is made up of whey protein supplements (20g/d) and dietary pattern modification.
whey protein intervention
This group received dietary guidance and whey protein intervention for 12 weeks
whey protein
The intervention is made up of whey protein supplements (20g/d) and dietary pattern modification.
symbiotic placebo
The intervention is made up of maltodextrin (20g/d) and dietary pattern modification.
control
This group received dietary guidance and maltodextrin for 12 weeks
symbiotic placebo
The intervention is made up of maltodextrin (20g/d) and dietary pattern modification.
whey protein placebo
The intervention is made up of maltodextrin (20g/d) and dietary pattern modification.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
symbiotic
The intervention is made up of multiple probiotics and prebiotics (20g/d) and dietary pattern modification.
whey protein
The intervention is made up of whey protein supplements (20g/d) and dietary pattern modification.
symbiotic placebo
The intervention is made up of maltodextrin (20g/d) and dietary pattern modification.
whey protein placebo
The intervention is made up of maltodextrin (20g/d) and dietary pattern modification.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Can cooperate with the measurement and questionnaire survey
3. Meets Asian Working Group for Sarcopenia (AWGS) 2019 diagnostic criteria for sarcopenia
4. Obtain informed consent to participate in this study
Exclusion Criteria
2. Suffers from neuromuscular related diseases
3. Immobility
4. Have taken antibiotics, probiotics and other medications that may affect the gut microbiota in the last 6 weeks
5. Implants of electronic devices or metal objects in the body
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Peking Union Medical College Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yu Kang, MD
Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Peking Union Medical College Hospital
Beijing, Beijing Municipality, China
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Gut-Intervention-SAR-2024
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.