CClinicalTrials.gg
CompletedNCT05549622Updated Jul 18, 2025

Impact of Diet on the Gut-Muscle Axis in Older Adults

An interventional study of Low-soluble fiber diet and High-soluble fiber diet in Sarcopenia, Dietary Exposure and Microbial Colonization, sponsored by Tufts University. Completed at 1 site in United States. Open to participants aged 65 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-07-18.

Sponsored by Tufts University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
31
Allocation
Randomized
Ages
65 Years and older
Sex
All
01

Study summary

Muscle health declines during aging. One factor that may impact muscle health is the community of bacteria that live in our intestines, but studies aimed at improving muscle health by targeting the gut in older adults are sparse. The primary goal of this study is to use a diet that is enriched in soluble fiber, which is exclusively utilized by gut bacteria to make substances that can impact muscle health, to improve muscle-related measures in older adults.

Read the detailed description

During aging, skeletal muscle mass and physical function decrease, whereas levels of lipids and adipocytes increase within and between muscle cells, thereby worsening muscle composition. As a result of these age-related changes, older adults are at a higher risk for frailty, falls and fracture, disability and hospitalization, and all-cause mortality. Accordingly, elucidation of mechanisms that underlie muscle mass, muscle composition, and physical function, and interventions that positively affect these variables will be important for addressing the public health priority of an improved quality of life and healthy aging in older adults.

The gut microbiome and its metabolic products are involved in mechanisms that impact skeletal muscle mass, muscle composition, and physical function, which has been defined as the gut-muscle axis. For example, muscle mass and physical function are reduced in animals that do not have a microbiome (germ-free mice), and in antibiotic-treated mice, an intervention that reduces gut bacterial content. Investigating further, gut bacteria-derived metabolites affect muscle mass, muscle composition, and physical function in young and aged animals, including positive effects for the short-chain fatty acids (SCFAs) acetate, propionate, and butyrate, and negative effects for indoxyl sulfate (IS) and para-cresol sulfate (PCS). Similarly, phenol sulfate (PS) and phenylacetylglutamine (PAG) are gut microbiome-derived metabolites that were associated with poor muscle composition and worse physical function in studies of older adult humans that were published by our group. Interestingly, higher colonic levels of SCFAs are associated with a lower pH, an important finding because growth of Enterobacteriaceae, a bacterial family that contains genes involved in the production of IS, PCS, PS, and PAG, is limited in an acidic environment and following exposure to physiological levels of SCFAs. Taken together, these data suggest that interventions aimed at increasing bacterial SCFA production may be an important approach for improving muscle-related measures in older adults.

Soluble fiber fermentation by gut bacteria results in the formation of acetate, propionate, and butyrate, and fecal SCFAs proportionally increase, whereas circulating levels of IS and PCS are reduced in response to high-soluble fiber diets. As a proof of concept, fecal and circulating levels of SCFAs, muscle mass, and aerobic exercise capacity were increased in young mice that were fed a relatively higher soluble fiber diet, but few studies have attempted this approach in older adult humans. When considering that fecal levels of SCFAs decrease during aging, whereas plasma levels of IS, PCS, PS, and PAG increase, these data collectively suggest that a high-soluble fiber diet may be an important approach for improving muscle-related measures in older adults humans. To test this hypothesis, older adults will be randomized to consume a high- or low-soluble fiber diet for 12-weeks.

02

Conditions studied

  • Sarcopenia
  • Dietary Exposure
  • Microbial Colonization

Keywords

  • skeletal muscle
  • soluble fiber
  • gut-muscle axis
  • microbiome
  • SCFA
  • Uremic metabolites
03

In context

Sarcopenia

1,208 studies on the registry are indexed under Sarcopenia; 402 are open to participants now.

This study's enrollment of 31 is below the median of 60 across 775 interventional studies indexed under Sarcopenia.

Browse Sarcopenia studies →

Lead sponsor

Tufts University is the lead sponsor of 225 studies on the registry; 24 are open to participants now.

Of its 10 completed or terminated interventional studies of FDA-regulated products, 7 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Independently living older adults (> 65y)
  2. Sedentary (Godin-Shepard Leisure Time Physical Activity Questionnaire score \< 10)
  3. Non-smoking
  4. Not already consuming a high-fiber diet (> 22, 28 g/day for women, men)
  5. Free of gastrointestinal disease (gastrointestinal cancer, inflammatory bowel disease, bariatric surgery, irritable bowel syndrome)
  6. Fluent in English
  7. Willing to attend three study visits (enrollment, baseline, and week-13)
  8. Willing to consume an abundance of fruits, vegetables, nuts/seeds
  9. Willing to consume an abundance of soluble fiber-rich foods (broccoli, brussels sprouts, flaxseeds sweetened with dates, lima beans, butternut squash, carrots, collard greens)
  10. Willing to tolerate mild gastrointestinal discomfort (bloating, belly grumbling, flatulence). Note that all attempts will be made to replace foods that may trigger these issues.
  11. Willing to not consume antibiotics during the 13-week study
  12. Willing to not schedule a colonoscopy during the 13-week study

Exclusion criteria

Exclusion Criteria:

  1. Unwilling to visit the Tufts Human Nutrition Research Center on Aging (HNRCA) 3x/week to pick up the pre-prepared study diet
  2. Unwilling to only consume the provided food (unsweetened tea and/or black coffee are allowed)
  3. Food allergies related to foods that are included in the study
  4. Chewing problems
  5. Unwilling to wear a daily step counter (pedometer)
  6. Unwilling to complete a daily questionnaire that will assess gastrointestinal comfort
  7. Malnutrition (BMI \< 18.5 kg/m2)
  8. Use of supplemental probiotics or antibiotics, participation in an investigational drug evaluation, or a recent change in habitual medication use within the 1 month-period prior to the screening visit
  9. > 5% weight loss or weight gain within the past 6-months
  10. A recent history of alcohol abuse (within the past 5 years)
  11. A history of any significant injury or surgery that currently affects physical functioning and ability to perform physical function testing
  12. Treatment with immunosuppressive drugs
  13. A prior diagnosis of organ failure (heart, liver, renal, respiratory)
  14. Diabetes mellitus (type 1, or type 2 with insulin therapy)
  15. Chronic kidney disease (eGFR ≤ 30 mL/min/1.73 m2)
  16. Overt disease (cancer, dementia, cardiovascular disease)
  17. Chronic use of anti-inflammatory medication (corticosteroids)
  18. Already enrolled in another research study
  19. Active infection, including Tuberculosis , HIV, malaria, hepatitis, shingles, Methicillin-Resistant Staphylococcus Aureus (MRSA), SARS-CoV-2
  20. Any major illness or condition that may interfere with study outcomes at the discretion of the study physician
  21. Won't remain in Boston for the 13-week study duration
  22. Unwilling to complete a daily checklist aimed at quantifying the amount of food eaten on the study diet
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
31 participants (actual)

Study arms

  • Other
    Low-soluble fiber diet

    Other: Low-soluble fiber diet

  • Active comparator
    High-soluble fiber diet

    Other: High-soluble fiber diet

Interventions

  • OtherLow-soluble fiber diet

    12 older adults (\>65y) will be randomized to consume the USDA Guidelines for fiber intake (10g of total fiber/1000 calories), as the low-soluble fiber diet

  • OtherHigh-soluble fiber diet

    12 older adults (\>65y) will be randomized to consume 34-35g of total fiber/1000 calories, as the high-soluble fiber diet

06

What researchers measure

Primary outcomes

  1. Quantification of SCFAs in fecal samples

    Fecal levels of bacterial metabolites, including acetate, propionate, and butyrate will be determined at the baseline and week-13 study visits

    Time frame: Change from baseline when compared with the Week-13 visit

  2. Quantification of whole-body lean mass with DXA

    Measurement of whole-body lean mass will be determined at the baseline and week-13 study visits

    Time frame: Change from baseline when compared with the Week-13 visit

  3. Quantification of hand grip strength

    Grip strength will be determined at the baseline and week-13 study visits

    Time frame: Change from baseline when compared with the Week-13 visit

  4. Chair stand test

    The number of chair stands that can be performed in 30 seconds will be determined at the baseline and week-13 study visits

    Time frame: Change from baseline when compared with the Week-13 visit

Secondary outcomes

  1. Quantification of thigh muscle composition with computed tomography

    Determined at the baseline and week-13 study visits

    Time frame: Change from baseline when compared with the Week-13 visit

  2. 6-minute walk test

    The distance walked in 6 minutes will be determined at the baseline and week-13 study visits

    Time frame: Change from baseline when compared with the Week-13 visit

  3. Quantification of gut bacterial metabolites in plasma

    Bacterial metabolites, including SCFAs but also indoxyl sulfate, p-cresol sulfate, phenol sulfate, and phenylacetylglutamine will be determined at the baseline and week-13 study visits

    Time frame: Change from baseline when compared with the Week-13 visit

  4. Quantification of gut bacterial composition in fecal samples

    Determined at the baseline and week-13 study visits

    Time frame: Change from baseline when compared with the Week-13 visit

  5. Quantification of pH in fecal samples

    Determined at the baseline and week-13 study visits

    Time frame: Change from baseline when compared with the Week-13 visit

07

Study locations

1 site
  • Jean Mayer Human Nutrition Research Center on Aging at Tufts University
    Boston, Massachusetts 02111, United States
08

References and documents

Individual participant data

Plan to share: No — No data from participants will be shared with researchers not affiliated with this project.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05549622
Lead sponsor
Tufts University
Responsible party
Jennifer Lee (Principal Investigator, Tufts University) — Principal investigator
First posted
Sep 22, 2022
Start date
Mar 1, 2023
Primary completion
Apr 30, 2025
Completion
Apr 30, 2025
Last update
Jul 18, 2025

Study contacts

Michael S Lustgarten, PhD
study director · Scientist II, NEPS Laboratory

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion