CClinicalTrials.gg
CompletedNCT07256314Updated Dec 5, 2025

Linking Dietary Nutrition, Dietary Patterns, Gut Microbiota, and Bone Density: A Cross-Sectional Study

An observational study in Bone Density and Gut Microbiomes, sponsored by Jianhua Ma. Completed at 1 site in China. Open to participants aged 6 Years to 13 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-12-05.

Sponsored by Jianhua Ma · Observational

Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
431
Ages
6 Years to 13 Years
Sex
All
01

Study summary

The study aims to understand the current situation of bone health in the Gannan Tibetan primary school student population, to explore the relationship between nutrition, intestinal microorganisms and bone health, to analyze the main factors affecting bone health from the perspective of nutrition and intestinal microecology, and to provide theoretical basis for the promotion and improvement of bone health in Tibetan primary school students.

02

Conditions studied

  • Bone Density
  • Gut Microbiomes
03

In context

Lead sponsor

Jianhua Ma is the lead sponsor of 2 studies on the registry; 1 is open to participants now.

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

04

Who can participate

Ages eligible
6 Years to 13 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

This study is based on a cross-sectional design. Two schools were selected: one rural primary school in Xiahe County, Gannan Tibetan Autonomous Prefecture, and one urban primary school in Hezuo City, Gansu Province. Within the selected schools, a stratified random cluster sampling method was used to randomly select one class from each grade as the study subjects.

Eligibility criteria

Inclusion Criteria:

  • Tibetan primary school students currently enrolled in schools in Gannan Tibetan Autonomous Prefecture;

Willing to participate and able to cooperate in completing bone density measurements;

Additional inclusion criteria: Subjects who are 9 years old or older and agree to participate in dietary surveys and fecal sampling.

Exclusion Criteria:Use of corticosteroid medications within the past year;

Suffering from skeletal system diseases, metabolic disorders, or endocrine diseases;

Additional exclusion criteria: Subjects who have used antibiotics in the past three months and are undergoing fecal sampling.

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05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
431 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Good Bone Density group and normal bone density group

    Other: No Intervention: Observational Cohort

Interventions

  • OtherNo Intervention: Observational Cohort

    No Intervention

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What researchers measure

Primary outcomes

  1. Dietary Characteristics

    Dietary data were collected using a food frequency questionnaire (FFQ) to analyze dietary patterns and nutrient intake.

    Time frame: Day 1

  2. Bone density test

    In this study, a peripheral dual-energy X-ray absorptiometry (EXA-PRESTO) was used to measure the bone density of the non-dominant forearm of the subjects.

    Time frame: Day1

  3. Fecal sample microbiological testing and analysis

    This study entrusted Tianhao Gene Technology Co., Ltd. to perform the intestinal microbiome Accu16STM (16S rRNA absolute quantitative sequencing). The main research processes include DNA extraction, PCR amplification, library construction, and sequencing.

    Time frame: Day 1

07

Study locations

1 site
  • Lanzhou university
    Lanzhou, Gansu 730000, China
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References and documents

Individual participant data

Plan to share: No

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 Dec 5, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07256314
Lead sponsor
Jianhua Ma
Responsible party
Jianhua Ma (Lecturer, LanZhou University) — Sponsor-investigator
First posted
Dec 1, 2025
Start date
Oct 10, 2023
Primary completion
Mar 31, 2025
Completion
Mar 31, 2025
Last update
Dec 5, 2025

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 Nov 2025. You cannot join it, but the record below documents what was studied.

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