IMPROVE: Evaluation of a combined lifestyle intervention program to improve quality of life in long-term ICU-survivors
Recruiting
- Conditions
- Post-intensive care syndroomRecovery after critical illness
- Registration Number
- NL-OMON49292
- Lead Sponsor
- Medisch Centrum Leeuwarden
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 40
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 < 67%
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Physical functioning (subscale score of the RAND-36) at the end of the 12 week<br /><br>intervention period.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Hand grip strength test<br /><br>Six-minute walking test<br /><br>Ultrasound measurements of the quadriceps muscle<br /><br>Morton mobility index<br /><br>Dietary intake<br /><br>Health-related quality of life (RAND-36, complete questionnaire)<br /><br>Hospital Anxiety and Depression Scale (HADS)<br /><br>Cognitive Failure Questionnaire (CFQ)<br /><br>Happiness Index (HI)<br /><br><br /><br>All endpoints are assessed after the 12 week intervention period.</p><br>