Early Rehabilitation After Hip Fracture
Primary Purpose
Accidental Falls, Fractures, Hip Fractures
Status
Unknown status
Phase
Phase 3
Locations
Switzerland
Study Type
Interventional
Intervention
cholecalciferol
Physiotherapy
Sponsored by
About this trial
This is an interventional prevention trial for Accidental Falls focused on measuring Vitamin D, Elderly, Hip fracture, Falls, Physical Therapy, Disability
Eligibility Criteria
Inclusion Criteria: Age 65 years or older Acute hip fracture admitted to one hospital center Exclusion Criteria: A Folstein Mini Mental Score of less than 15 as an indicator of significant dementia Primary hyperparathyroidism Current cancer with wasting or bone metastases Hyperparathyroidism Sarcoidosis A kidney stone in the past 5 years or significant renal disease (creatinine clearance below 15 ml/min) Hypercalcemia (albumin adjusted) of more than 2.8 mmol/l non-surgical treatment no German language skills severe hearing or visual impairment
Sites / Locations
- Triemli HospitalRecruiting
Outcomes
Primary Outcome Measures
rate of falls compared between treatment arms
Secondary Outcome Measures
rate of injurious falls
number of persons who fell
low-trauma fractures (at the hip, forearm, humerus, pelvis, ankle, spine, femur, tibia)
disability
quality of life (Euro-Qol)
mortality
health care utilization
admission to nursing home compared between treatment arms among subjects, who are community-dwelling prior to the index hip fracture
Full Information
NCT ID
NCT00133640
First Posted
August 22, 2005
Last Updated
September 7, 2006
Sponsor
Swiss National Science Foundation
1. Study Identification
Unique Protocol Identification Number
NCT00133640
Brief Title
Early Rehabilitation After Hip Fracture
Official Title
Early Rehabilitation After Hip Fracture: A Randomized Controlled Trial Comparing Different Vitamin D and Rehabilitation Programs
Study Type
Interventional
2. Study Status
Record Verification Date
August 2006
Overall Recruitment Status
Unknown status
Study Start Date
January 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2008 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Swiss National Science Foundation
4. Oversight
5. Study Description
Brief Summary
The aim of this study is to compare a low versus high intensity physiotherapy early rehabilitation program combined with a low versus high dose vitamin D early rehabilitation program in a randomized controlled trial among elderly patients with acute hip fracture in an acute care setting. The primary outcome to be compared between treatment arms is the rate of falls during a 12-month follow-up. Secondary outcomes are injurious falls, number of persons who fell, low-trauma fractures (at the hip, forearm, humerus, pelvis, ankle, spine, femur, tibia), disability, quality of life (Euro-Qol), mortality and health care utilization. Another secondary outcome will be admission to nursing home compared between treatment arms among subjects, who are community-dwelling prior to the index hip fracture. Admission to nursing home is the marker of loss of independence for the individual, but also triggers high cost for the society.
The study will provide new early rehabilitation guidelines to allocate health care resources efficiently in the acute care setting. Eventually and most importantly, the study will help improve outcomes in patients with hip fractures.
Detailed Description
Subjects:
The researchers will enroll 204 elderly subjects (men and women) admitted to two large hospital centers with acute hip fracture. Subjects may be institutionalized or community-dwelling prior to admission. To be enrolled in the study subjects need to be 65 years or older. Demented persons, who reach a Folstein Mini Mental Status of less than 15 are excluded.
Design:
Once written informed consent from participants or proxies is given, subjects will be randomly assigned to 4 different program combinations based on a 2X2 factorial design: (1) low dose vitamin D / low intensity physiotherapy; or (2) low dose vitamin D / high intensity physiotherapy; or (3) high dose vitamin D / low intensity physiotherapy; or (4) high dose vitamin D / high intensity physiotherapy. Low dose Vitamin D is 800 IU cholecalciferol per day and high dose vitamin D is 2000 IU cholecalciferol per day.
Subjects will be recruited within 5 days after hip fracture surgery and followed for adverse outcomes over a 12-month period. Dose of vitamin D will be double-blinded.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Accidental Falls, Fractures, Hip Fractures
Keywords
Vitamin D, Elderly, Hip fracture, Falls, Physical Therapy, Disability
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
Double
Allocation
Randomized
Enrollment
204 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
cholecalciferol
Intervention Type
Behavioral
Intervention Name(s)
Physiotherapy
Primary Outcome Measure Information:
Title
rate of falls compared between treatment arms
Secondary Outcome Measure Information:
Title
rate of injurious falls
Title
number of persons who fell
Title
low-trauma fractures (at the hip, forearm, humerus, pelvis, ankle, spine, femur, tibia)
Title
disability
Title
quality of life (Euro-Qol)
Title
mortality
Title
health care utilization
Title
admission to nursing home compared between treatment arms among subjects, who are community-dwelling prior to the index hip fracture
10. Eligibility
Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 65 years or older
Acute hip fracture admitted to one hospital center
Exclusion Criteria:
A Folstein Mini Mental Score of less than 15 as an indicator of significant dementia
Primary hyperparathyroidism
Current cancer with wasting or bone metastases
Hyperparathyroidism
Sarcoidosis
A kidney stone in the past 5 years or significant renal disease (creatinine clearance below 15 ml/min)
Hypercalcemia (albumin adjusted) of more than 2.8 mmol/l
non-surgical treatment
no German language skills
severe hearing or visual impairment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Heike A Bischoff-Ferrari, MD, MPH
Phone
+41-44-2552699
Email
Heike.Bischoff@usz.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heike A Bischoff-Ferrari, MD, MPH
Organizational Affiliation
University of Zurich
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Robert Theiler, MD
Organizational Affiliation
Triemli Spital Zurich
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Hannes B Staehelin, MD
Organizational Affiliation
University of Basel
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Andreas Platz, MD
Organizational Affiliation
TriemliSpital
Official's Role
Study Director
Facility Information:
Facility Name
Triemli Hospital
City
Zurich
ZIP/Postal Code
8063
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Heike A Bischoff-Ferrari, MD, MPH
Phone
+41-44-2552699
Email
HeikeBischoff@usz.ch
First Name & Middle Initial & Last Name & Degree
Robert Theiler, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
30941485
Citation
Fischer K, Trombik M, Freystatter G, Egli A, Theiler R, Bischoff-Ferrari HA. Timeline of functional recovery after hip fracture in seniors aged 65 and older: a prospective observational analysis. Osteoporos Int. 2019 Jul;30(7):1371-1381. doi: 10.1007/s00198-019-04944-5. Epub 2019 Apr 2.
Results Reference
derived
PubMed Identifier
28974464
Citation
Nardi M, Fischer K, Dawson-Hughes B, Orav EJ, Meyer OW, Meyer U, Beck S, Simmen HP, Pape HC, Egli A, Willett WC, Theiler R, Bischoff-Ferrari HA. Association between Caregiver Role and Short- and Long-Term Functional Recovery after Hip Fracture: A Prospective Study. J Am Med Dir Assoc. 2018 Feb;19(2):122-129. doi: 10.1016/j.jamda.2017.08.009. Epub 2017 Sep 30.
Results Reference
derived
PubMed Identifier
22705148
Citation
Schaller F, Sidelnikov E, Theiler R, Egli A, Staehelin HB, Dick W, Dawson-Hughes B, Grob D, Platz A, Can U, Bischoff-Ferrari HA. Mild to moderate cognitive impairment is a major risk factor for mortality and nursing home admission in the first year after hip fracture. Bone. 2012 Sep;51(3):347-52. doi: 10.1016/j.bone.2012.06.004. Epub 2012 Jun 12.
Results Reference
derived
PubMed Identifier
20458090
Citation
Bischoff-Ferrari HA, Dawson-Hughes B, Platz A, Orav EJ, Stahelin HB, Willett WC, Can U, Egli A, Mueller NJ, Looser S, Bretscher B, Minder E, Vergopoulos A, Theiler R. Effect of high-dosage cholecalciferol and extended physiotherapy on complications after hip fracture: a randomized controlled trial. Arch Intern Med. 2010 May 10;170(9):813-20. doi: 10.1001/archinternmed.2010.67.
Results Reference
derived
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Early Rehabilitation After Hip Fracture
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