ProMuscle 65PK: feasibility and potential impact of a physical activity and nutrition intervention in practice for community dwelling elderly people receiving home care: A pilot study

ProMuscle 65PK: feasibility and potential impact of a physical activity and nutrition intervention in practice for community dwelling elderly people receiving home care: A pilot study - ProMuscle 65PK pilot study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON42268

Enrollment

Registered

2015-04-21

Start date

2015-04-07

Completion date

Unknown

Last updated

2024-04-23

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

Conditions

Zorgbehoevende (kwetsbare) ouderen frailty Physical impairment

Interventions

For twelve weeks, subjects will receive the ProMuscle 65PK intervention. All participants will perform both resistance exercise and increase their protein intake during the study. Subjects perform p

during performance of the exercises there is always one-on-one guidance. The trainings start with a warming-up, followed by exercises for the major muscles, and a cooling-down. The training intensit

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: In order to participate in the study, individuals should be aged 65 years of over, living in the municipality of Harderwijk, being able to understand Dutch, and have a care referral for at least one of the following types of care: - Domestic care - Personal care - Nursing care - Individual or group support

Exclusion criteria

Exclusion criteria: The General Practitioner of the possible participant will check whether a person can safely participate in the study, based on the following exclusion criteria:;- Allergic or sensitive to milk proteins en/or lactose - Clients with diagnosed COPD or cancer - Clients with diabetes type I or type II that are unstable, not well regulated with medication, or do not notice when they get hypoglycaemia - Clients with hypertension (systolic blood pressure >160 mmHG) that is not well regulated met medication - Clients with severe heart failure - Clients with renal insufficiency (eGFR

Design outcomes

Primary

Measure	Time frame
The primary study outcomes focus on the feasibility of implementing the intervention in practice (process evaluation): - Acceptability of the intervention (participants and professionals) - Applicability of the intervention (professionals) - Implementation integrity: Extent to which the intervention is implemented as planned in the implementation protocols (professionals) - Dose received: The compliance of the participants to the trainings, and whether the protein intake during the main meals is increased to 25 grams (participants) - Factors for success and failure	—

Measure

Time frame

The primary study outcomes focus on the feasibility of implementing the intervention in practice (process evaluation): - Acceptability of the intervention (participants and professionals) - Applicability of the intervention (professionals) - Implementation integrity: Extent to which the intervention is implemented as planned in the implementation protocols (professionals) - Dose received: The compliance of the participants to the trainings, and whether the protein intake during the main meals is increased to 25 grams (participants) - Factors for success and failure

—

Secondary

Measure	Time frame
The secondary study outcomes are the changes after 12 weeks in the following outcomes (participants): - Muscle mass - Muscle strength - Physical functioning - Activities of daily living (ADL) - Quality of life - Dietary intake	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)