Ignite Creation Date:
2024-05-05 @ 6:39 PM
Last Modification Date:
2024-10-26 @ 9:35 AM
Study NCT ID:
NCT00523575
Status:
COMPLETED
Last Update Posted:
2011-07-20
First Post:
2007-08-29
Brief Title:
Nutritional Intervention in Hip Fracture Patients
Sponsor:
Maastricht University Medical Center
Organization:
Maastricht University Medical Center
Study Overview
Official Title:
Effectiveness and Cost-effectiveness of Nutritional Screening and Intervention in Elderly Subjects After Hip Fracture
Status:
COMPLETED
Status Verified Date:
2011-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Hip fractures are highly prevalent and are expected to increase due to the ageing population Malnutrition is often present in these patients and is associated with prolonged convalescence lower mobility lower mental function lower quality of life and higher complication rate Nutritional intervention starting soon after hospital admission might reduce complication rate and total length-of-stay by improving nutritional and functional status Research questions are
1 Does nutritional intervention reduce total length-of-stay
2 Is nutritional intervention cost-effective
3 Can nutritional screening contribute to targeting of nutritional intervention and thereby reduce costs without loss of effectiveness
Patients randomized to the intervention group will receive oral nutritional supplements protein and energy enriched and regular dietetic counselling during hospitalisation and after discharge at patients homes for 3 months Patients in the control group will receive usual nurse and dietetic care Outcome measurements will be taken at baseline 3 months and 6 months after inclusion
1 Does nutritional intervention reduce total length-of-stay
2 Is nutritional intervention cost-effective
3 Can nutritional screening contribute to targeting of nutritional intervention and thereby reduce costs without loss of effectiveness
Patients randomized to the intervention group will receive oral nutritional supplements protein and energy enriched and regular dietetic counselling during hospitalisation and after discharge at patients homes for 3 months Patients in the control group will receive usual nurse and dietetic care Outcome measurements will be taken at baseline 3 months and 6 months after inclusion
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| ZonMw 80-007022-98-07510 | None | None | None |