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The VOILA Intervention Study

Vitality Oriented Innovation for the Lifecourse of the Ageing Society Intervention Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05354310
Acronym
VOILA
Enrollment
220
Registered
2022-04-29
Start date
2022-02-01
Completion date
2024-07-01
Last updated
2022-04-29

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

Conditions

Aging

Keywords

Resistance Training, Nutrition, Protein supplement, Gut microbiome, Immunometabolsim, Mobility

Brief summary

The multi-disciplinary and translational VOILA project presents a unique intersection between gut, immuno-metabolic, and musculoskeletal health. The main goals of the project are to develop biomarkers for healthy aging and prevent disease by maintaining quality of life in older adults. Within this umbrella project, the multimodal VOILA lifestyle intervention study will assess the impact of a twelve-week strength training and nutritional intervention in older adults with different degrees of mobility. The study will improve the current understanding of the complex relationship between gut and muscle health in different segments of mobility and obtain an insight into the heterogeneity of responsiveness between individuals.

Interventions

COMBINATION_PRODUCTVOILA

Participants will be given dietary supplement powder containing protein, galactooligosaccharide (GOS), vitamin D, and calcium throughout the twelve weeks of intervention. This will be accompanied with a resistance training regime whereby participants will train three times a week for the three months. A variety of measurements will be carried out at baseline and at endline.

Sponsors

Maastricht University Medical Center
CollaboratorOTHER
Wageningen University and Research
CollaboratorOTHER
FrieslandCampina
CollaboratorINDUSTRY
ZonMw: The Netherlands Organisation for Health Research and Development
CollaboratorOTHER
Leiden University Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
70 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age ≥70 years * A body mass index of 18.5-35.0 kg/m2 * Able to give written informed consent * Community-dwelling * Mentally competent with a Mini-Mental State Examination (MMSE) score of ≥24 points * Able to follow the study protocol Additional group-specific criteria: Metabolically compromised group \- Framingham Risk Score ≥14 and Metabolomic Mortality Score of ≥0.173 Reduced mobility group - People able to walk but needing walking aids to walk anywhere outside their house Total knee replacement intervention and control group \- Discharged from MUMC+ after undergoing elective knee replacement surgery (intervention starts \ 4 weeks after surgery) Active reference group * People who meet the Nederlandse Norm Gezond Bewegen. This means they partake in at least moderate exercise for at least 30 minutes on 5 days of the week, as determined by the SQUASH questionnaire (40). * Framingham Risk Score of \<14 and Metabolic Mortality Score of \<0.173

Exclusion criteria

* Already using prebiotic fibres\* * Use of laxatives\* * Not willing to stop using dietary supplements in high doses (high doses: 0.10\*Upper Level or more)\* * Following a structured, intense exercise programme (currently or in the last year)\* * Allergic, intolerant or hypersensitive to milk/lactose (self-reported)\* * Dietary restrictions on milk/lactose/prebiotics/vitamin D/calcium consumption\* * Abnormal hepatic or renal laboratory parameters (estimated glomerular filtration rate (eGFR) \<30 ml/min/1.73 m2 (screening) or contra-indication by treating medical practitioner (data from hospital) * Diagnosis of disorders/diseases in which a high protein intake can be harmful, such as renal impairment or failure, liver disease, or diabetes associated with nephropathy (treating medical practitioner has the decisive voice). * Diseases, conditions or disorders which may affect the ability to follow the study protocol and which cannot be overcome with help of a caregiver Any other medical condition that may interfere with the safety of the participants during training or assessment of the outcome parameters, in the investigators' judgement * Current participation in other scientific research that conflicts with this study (e.g. intervention studies or weight management studies) * Not signed up to a general practitioner * No permission to request information from the general practitioner/ treating specialist(s) about medical history, medication use. Specific for TKR group: * Referral to rehabilitation facility after hospital discharge * Osteoarthritis of the knee secondary to septic arthritis, osteonecrosis, fracture, osteochondritis dissecans, or malignant processes * Collagen disorders, e.g. Marfan and Ehler-Danlos * Total hip prosthesis or TKR in both legs

Design outcomes

Primary

MeasureTime frameDescription
Muscle mass10 weeksappendicular lean mass in kg (DEXA)
Muscle function10 weeks5-times repeated chair rise test in seconds
Gut health10 weeksbifidobacteria (from stool sample) in log10 cells per gram dried faeces
Immuno-metabolic health - GLC10 weeksfasting blood glucose (GLC) in mmol/L
Immuno-metabolic health - GlycA10 weeksglycoprotein acetyls (GlycA) in mmol/L
Immuno-metabolic health - VLDL10 weeksvery low-density lipoprotein (VLDL)-diameter in nm (from Nightingale 1H NMR platform)

Secondary

MeasureTime frameDescription
Body composition - Regional lean mass10 weeksDEXA regional lean mass in kg
Body composition - Regional fat mass10 weeksDEXA regional fat mass in kg
Immuno-metabolic health - Hba1c10 weekshaemoglobin A1c (Hba1c)
Muscle function - SPPB10 weeksShort Physical Performance Battery (SPPB)
Immuno-metabolic health - Blood pressure10 weeksBlood pressure in mmHg
Knee replacement group additional outcomes - CT10 weeksSingle-slice CT-scans midway the upper legs
Knee replacement group additional outcomes - WOMAC10 weeksWestern Ontario and McMaster Universities Arthritis Index (WOMAC).
Immuno-metabolic health - Insulin10 weeksInsulin in mol/L
Muscle function - TUG10 weeksTimed Up and Go test (TUG)
Muscle function - 6MWT10 weeks6-minute walking test (6MWT)
Muscle function - 1RM10 weeks1 repetition maximum test (1RM) as measured on exercise machines
Body composition - Whole body regional lean mass10 weeksDEXA whole body lean mass in kg
Body composition - Whole body regional fat mass10 weeksDEXA whole body fat mass in kg

Countries

Netherlands

Contacts

Primary ContactP. Eline Slagboom, PhD
P.Slagboom@lumc.nl0653879941
Backup ContactJordi Morwani Mangnani, MSc
j.morwani_mangnani@lumc.nl

Outcome results

None listed

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