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TEAMS - Training and protein recommendations for frail older adults (Part I: community-dwelling)

TEAMS - Training and protein recommendations for frail older adults (Part I: community-dwelling) - TEAMS - I

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON54919
Enrollment
300
Registered
2021-02-09
Start date
2021-04-08
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Ondervoeding & Geriatrische syndromen (zoals sarcopenie) Sarcopenia and malnutrition

Interventions

Control group receiving intervention: - Resistance exercise training, twice weekly for 12 weeks in which subjects will be randomized by intensity (%1RM) - Regular health care (+ information flyer) I

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: * Community-dwelling older adult, receiving in-home care services * Aged 65 or older * Physical ability and willingness to execute a resistance exercise program * Ability and willingness to comply with the protocol * Willingness that general practitioner will be notified on study participation * Written informed consent * Consent of the study physician (ability to comply with the protocol in the opinion of the study physician, to ensure safety for the participants)

Exclusion criteria

Exclusion criteria: * Inability to understand the Dutch language * Cognitive impairment (MMSE 3) * Diagnosed degenerative neurocognitive disorders * COPD GOLD >3 * Use of total parenteral nutrition (TPN) * Active medical treatment interfering with this intervention (e.g. cancer patients following systemic and immune therapy) * Physical disabled (walking aids or mild visual impairment are not an exclusion criteria) * Current enrollment in a fixed rehabilitation program or other intervention studies * Palliative treatment or a life expectancy of

Design outcomes

Primary

MeasureTime frame
The primary outcome is the change in muscle strength between baseline and twelve- weeks, and is accessed with a one repetition maximum tests (1-RM).

Secondary

MeasureTime frame
- social demographic characteristics - medical history / medication use - cognitive ability - body composition - muscle architecture - inflammation markers, glucose and insulin levels - physical performance - handgrip strength - activities of daily living - quality of life - malnutrition - daily dietary intake - daily physical activity - cognitive performance - psychosocial outcomes - sleep quality - cost-effectiveness - adverse events / medical status - adherence - process evaluation

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: May 17, 2026