ClinicalTrials.gg
RecruitingNCT07753291Updated Sep 1, 2026

The Effects of the Yi Jin Jing on the Muscles and Bones of Adults

An interventional study of Yijinjing in Musculoskeletal Health and Healthy Adult Volunteers, sponsored by Beijing Hospital of Traditional Chinese Medicine. Recruiting at 1 site in China. Open to participants aged 18 Years to 90 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-01.

Sponsored by Beijing Hospital of Traditional Chinese Medicine · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Not applicable
Ages
18 Years to 90 Years
Sex
All
01

Study summary

Observation of the effects of Yi Jin Jing on the muscles and bones of adults

02

Conditions studied

  • Musculoskeletal Health
  • Healthy Adult Volunteers

Keywords

  • Yijinjing
  • Healthy Adult Volunteers
  • Musculoskeletal Health
03

In context

Lead sponsor

Beijing Hospital of Traditional Chinese Medicine is the lead sponsor of 22 studies on the registry; 12 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18-90 years inclusive;
  • Generally healthy, no acute or chronic diseases affecting major organ functions;
  • No cognitive impairment, able to understand and comply with study procedures;
  • Willing and able to provide written ;
  • No pregnancy or lactation (for females);
  • No recent (within 3 months) major surgery, hospitalization, or significant weight change (>5% body weight).

Exclusion criteria

Exclusion Criteria:

  • Presence of acute or unstable chronic diseases (e.g., uncontrolled hypertension, diabetes, heart failure, or );
  • Severe cognitive impairment, psychiatric disorders, or inability to follow study instructions;
  • Recent (≤3 months) major surgery, trauma, or hospitalization;
  • Pregnancy, lactation, or without reliable ;
  • (BMI) \<16 or >40 kg/m²;
  • Current use of medications affecting muscle or nutritional metabolism (e.g., , anabolic steroids);
  • Participation in another interventional trial within 30 days.
Terms in these criteria, in plain language(6)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    The effects of Yi Jin Jing on the muscles and bones of adults

    Yijinjing exercise

    Behavioral: Yijinjing

Interventions

  • BehavioralYijinjing

    Yijinjing

06

What researchers measure

Primary outcomes

  1. Appendicular Skeletal Muscle Index

    Appendicular Skeletal Muscle Index (ASMI) = appendicular lean mass (kg) / height² (m²). It reflects muscle mass, used for sarcopenia diagnosis. Lower values indicate muscle loss, linked to aging, malnutrition, or disease.

    Time frame: Day 180 ± 10 days

Secondary outcomes

  1. Handgrip strength

    Handgrip strength (HGS) = maximum force (kg) measured by a dynamometer. It reflects overall muscle function, predicts disability, morbidity, and mortality. Low HGS indicates sarcopenia, frailty, or poor nutritional status.

    Time frame: Day 180 ± 10 days

  2. Nutrition intake form(MNA)

    Mini Nutritional Assessment - Short Form (MNA-SF) consists of 6 items: * Appetite and food intake - assesses whether food intake has decreased over the past 3 months. * Weight loss - records recent unintentional weight loss. * Mobility - determines whether the person can walk independently or is bedridden. * Acute disease or psychological stress - checks for stressful events in the past 3 months. * Neuropsychological problems - identifies dementia, depression, or other mental disorders that affect eating. * Body mass index (BMI) or calf circumference - reflects body fat reserves and muscle mass. Each item scores 0-3 points. A total score ≤11 indicates a risk of malnutrition. It is commonly used for nutritional screening in elderly populations.

    Time frame: Day 180 ± 10 days

  3. Fried

    Fried Frailty Phenotype = a 5-item scale assessing unintentional weight loss, exhaustion, low grip strength, slow walking speed, and low physical activity. item ≥3 = frail; 1-2 = prefrail; 0 = robust. Predicts falls, disability, and mortality.

    Time frame: Day 180 ± 10 days

  4. FRAIL

    FRAIL Scale = a 5-item questionnaire: Fatigue, Resistance (climb stairs), Ambulation (walk), Illness (≥5 chronic conditions), and Loss of weight (≥5%). Score 0 = robust, 1-2 = prefrail, 3-5 = frail. Quick screening for frailty in community settings.

    Time frame: Day 180 ± 10 days

  5. SPPB

    Short Physical Performance Battery (SPPB) = a 3-component test: standing balance (0-4), 4-meter gait speed (0-4), and 5-repetition chair stand (0-4). Total score 0-12; ≤8 indicates poor physical function, predicts disability, falls, and mortality in older adults.

    Time frame: Day 180 ± 10 days

  6. Muscle mass measured by ultrasound

    Ultrasound-based measurements of peripheral skeletal muscles offer a practical, non-invasive, and radiation-free approach for assessing muscle mass in clinical and research settings. In accordance with previously established cut-off values, the following parameters are employed to identify a tendency toward reduced muscle mass: 1. Biceps brachii cross-sectional area (CSA) - a male-specific indicator, with a value \< 7.1 cm² suggesting reduced muscle mass; 2. Tibialis anterior muscle thickness (MT) - a female-specific indicator, with a value \< 2.3 cm suggesting reduced muscle mass; 3. Rectus femoris muscle thickness (MT) - a gender-neutral rapid screening index, with a value \< 1.3 cm serving as a universal cut-off for both men and women, indicating a tendency toward low muscle mass. These ultrasonographic parameters are intended for initial screening and may assist in the early identification of individuals at risk for sarcopenia, particularly when access to dual-energy X-ray abs

    Time frame: Day 180 ± 10 days

07

Study locations

1 of 1 sites recruiting
  • No. 23, Ganju Road, Dongcheng District, Beijing
    Beijing, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Sep 2026; primary completion for Dec 2027, 15 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 4, 2026
First posted
Aug 7, 2026
StartEst.
Sep 1, 2026
Primary completionEst.
Dec 31, 2027
CompletionEst.
Dec 31, 2028
Last update
Sep 1, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07753291
Lead sponsor
Beijing Hospital of Traditional Chinese Medicine
Responsible party
He Jin (Investigator, Beijing Hospital of Traditional Chinese Medicine) — Principal investigator
First posted
Aug 7, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Dec 31, 2027 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
Sep 1, 2026

Study contacts

jin he hejin
Contact
17600765734@163.com
+8617600765734

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

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