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Move Study in Healthy Aging People

Effects of a Test Formula Milk Powder Combined With a Physical Activity Program on Mobility in Healthy Aging Subjects With Joint Discomfort

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02276183
Enrollment
55
Registered
2014-10-28
Start date
2015-04-30
Completion date
2016-08-31
Last updated
2016-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Joint Pain

Brief summary

Bone and muscle losses occur during ageing leading to increased risk of osteoporosis (there are more than 200 million people affected by osteoporosis worldwide), sarcopenia, loss of functionality and mobility. From around 45-50 years onwards, there is a progressive loss of muscle mass and strength (sarcopenia). This is partially due to an impairment of muscle protein synthesis in response to dietary proteins. Insufficient dietary protein may contribute to age-related loss of lean body mass (LBM) and strength which ultimately affects body movement. Key ingredients in selected investigational product are:Milk proteins, Calcium, Vitamin D, Vitamin C, Glucosamine Sulfate, Zinc. They have effects to improve physical mobility and functionality. The investigators expect improved effects of a nutritional intervention combined with a physical activity program on mobility in healthy aging subjects with joint discomfort.

Interventions

DIETARY_SUPPLEMENTNutrition intervention, test formula
BEHAVIORALprogressive physical activity

Tai Chi; dynamic strength training (knee extension, knee flexion, hip extension, side leg raise, plantar flexion); flexibility warm up and cool down (shoulder and upper arm stretch, hamstrings stretch, calf stretch, ankle stretch); aerobic fitness training(walking on even flat ground); balance training(standing on one foot; heel-to-toe walk; toe stand)

Sponsors

Société des Produits Nestlé (SPN)
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
45 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Target 45-65 y old * Suffering from (knee) pain. VAS on pain assessment \<= 4 on a range 0 to 10 * 20\<BMI\<28 * Time since menopause above 2y * iPAQ (International Physical Activity Questionnaire) score \<600

Exclusion criteria

* OA diagnosed * Medicine treatment * Chronic pain killers treatment for more than 7 consecutive days with a washout period of 2 weeks between 2 periods of treatment * Under corticoid, hormone (adrenal, thyroid) treatment * Traditional herbal medicine: in particular with claims on strengthening tendons and bones. This point will be included in FFQ (see annex) and evaluate. Subjects with chronic tablets supplementation ( calcium or drinking milk over 5 day wk-1 will be excluded, vitamin D, GS, or any with effect on bone and joints ) (set up a FFQ to specially investigate intakes of calcium tablets, milk and animal foods) * Pregnancy * Subject with knee/joint surgery/replacement and CLA (Cross Ligament) injury * History of relevant digestive disease, organic disease of heart, liver or kidney, severe function disorder of liver or kidney, metabolic/endocrine , neurological disease (e.g., Parkinson disease, stroke) with residual impairment, vertigo * Anaemia * Unable to carry out functional tests and questionnaires correctly (KOOS, physical activity) * Lower or upper extremity surgery or fracture in the last 3 months * Currently participating or having participated in another clinical trial in the three previous months

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in muscle extension isokinetic strength and 4 min speed stepBaseline and visit 7Change from baseline and muscle(quadriceps)extension isokinetic strength (peak torque) and 4 min speed step will be measured as the change of musculoskeletal functionality and mobitliy.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026