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IMPROVE: Evaluation of a combined lifestyle intervention program to improve quality of life in long-term ICU-survivors

IMPROVE: Evaluation of a combined lifestyle intervention program to improve quality of life in long-term ICU-survivors - IMPROVE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON49292
Enrollment
40
Registered
2020-10-22
Start date
2021-10-08
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Post-intensive care syndroom Recovery after critical illness

Interventions

The intervention group will be part of a 12-week combined lifestyle intervention encompassing group physical therapy twice a week and improvement of dietary caloric and protein intake by means of nu

Sponsors

Medisch Centrum Leeuwarden
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Long stay post-ICU patients (length of stay >=48h) between 6 weeks and 6 months after hospital discharge AND >18 years old AND able to visit the hospital 2 times a week AND a RAND-36 physical functioning subscale score

Exclusion criteria

Exclusion criteria: - Allergy to components of ProSource® - Inability to understand the Dutch language - Actively participating in a professional physical rehabilitation program during the study period. Note: previous participation in a concluded rehabilitation program is NOT an exclusion criterion.

Design outcomes

Primary

MeasureTime frame
Physical functioning (subscale score of the RAND-36) at the end of the 12 week intervention period.

Secondary

MeasureTime frame
Hand grip strength test Six-minute walking test Ultrasound measurements of the quadriceps muscle Morton mobility index Dietary intake Health-related quality of life (RAND-36, complete questionnaire) Hospital Anxiety and Depression Scale (HADS) Cognitive Failure Questionnaire (CFQ) Happiness Index (HI) All endpoints are assessed after the 12 week intervention period.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)