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Spitex-SpiTal-Autonomie-Reha-Kraft (STARK)

Primary Purpose

Osteoporosis, Frailty, Hip Fractures

Status
Terminated
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
STARK intervention
Standard of Care
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Osteoporosis focused on measuring Autonomy, Rehabilitation, Falls, Quality of life, Senior

Eligibility Criteria

70 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Community-dwelling prior to the hip fracture event
  • Living alone or with a partner/family member
  • Living in the city of Zurich
  • age 70+
  • Acute hip or pelvis fracture after minimal trauma (resulting from a fall occurring from a standard height and without the involvement of others or a vehicle)
  • Living at home without or with minimal (i.e. no more than 1x/day) support from the Spitex (ambulant nursing service) before the hip fracture
  • Participant is mentally competent (judicious) based on the treating physicians' opinion at the screening visit.
  • Inpatient rehabilitation or inpatient transitional care at a nursing home or ambulatory standard of care
  • The participant understands the study procedures and voluntarily agree to participate in the study and comply with all its procedures by giving written informed consent

Exclusion Criteria:

  • Patients who are expected to return home without help (i.e. no more care than Spitex 1x/day or physiotherapy 2x/week needed) directly after acute care are excluded.
  • Conservative treatment of acute hip fracture or surgical treatment that does not allow full weight bearing after surgery
  • Currently under cancer treatment or has active cancer (except for non-melanoma skin cancer)
  • Major visual or hearing impairment (visual and/or hearing aids are allowed) or other serious illness that would preclude participation
  • 24-hour nursing care need as this cannot be offered within the STARK package
  • Mobility impairment that precludes return to own apartment
  • Planned nursing home admission after acute hospital stay
  • Current participation in another clinical trial, or plans of such participation in the next 12 months (corresponding to the study duration)
  • Inability to read and/or speak German to an extent necessary to understand instructions and participate in the study
  • Unwilling to forego any additional vitamin D supplementation (bolus or regular intake).

Sites / Locations

  • Dept. of Geriatrics and Aging Research, University of Zurich / Geriatric Clinic University Hospital Zurich

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

STARK intervention

Standard Care

Arm Description

New care concept for hip fracture patients

Swiss standard of care for hip fracture patients

Outcomes

Primary Outcome Measures

Lower extremity function
Lower extremity function will be measured by the Short Physical Performance Battery (SPPB)

Secondary Outcome Measures

Gait speed
Gait speed will be obtained from the SPPB.
Gait speed
Gait speed will be assessed by a 400 m walk test.
Grip strength
Hand grip strength will be measured using a Martin Vigorimeter.
Repeated sit-to-stand
Repeated chair stand test will be obtained from the SPPB.
Rate of falls
Rate of falls will be assessed by a monthly phone call.
Health care utilization
Health care utilization will be assessed using the health care utilization questionnaire.
Number of re-hospitalizations
All hospitalizations will be documented as part of the safety documentation(SAE).
Number of nursing home admissions
All nursing home admissions will be documented.
Adherence to preventive strategies
Adherence will be documented by the Spitex staff.
Adherence to preventive strategies
Adherence will be documented by an adherence questionnaire.
Quality of life
Quality of life will be assessed by the RAND SF-36 questionnaire.
Quality of life
Quality of life will be assessed by the EuroQol (EQ-5D-3L) questionnaire.
Cognitive function
Cognitive function will be assessed by the MoCA.
Cognitive function
Cognitive function will be assessed by the MMSE.
Appendicular muscle mass
Appendicular muscle mass will be assessed by dual energy X-ray absorptiometry.
Bone mineral density
Bone mineral density will be assessed by dual energy X-ray absorptiometry.
Activities of daily living
Activities of daily living will be assessed by questionnaire (PROMIS-HAQ)

Full Information

First Posted
May 4, 2017
Last Updated
August 26, 2021
Sponsor
University of Zurich
Collaborators
Spitex Zürich, Switzerland, City of Zurich, Switzerland, University Hospital, Zürich, University of Applied Sciences of Western Switzerland, Ebnet Stiftung, Switzerland
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1. Study Identification

Unique Protocol Identification Number
NCT03154684
Brief Title
Spitex-SpiTal-Autonomie-Reha-Kraft
Acronym
STARK
Official Title
Efficacy of the STARK Comprehensive Autonomy Health Care Package in Functional Recovery After a Hip Fracture: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Terminated
Why Stopped
Insufficient Recruitment
Study Start Date
May 5, 2017 (Actual)
Primary Completion Date
August 15, 2021 (Actual)
Study Completion Date
August 15, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich
Collaborators
Spitex Zürich, Switzerland, City of Zurich, Switzerland, University Hospital, Zürich, University of Applied Sciences of Western Switzerland, Ebnet Stiftung, Switzerland

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary purpose of this study is to test if the STARK comprehensive autonomy health care package improves lower extremity function over time at 6 weeks, 3, 6 and 12 months after hip or pelvis fracture compared to the standard of care.
Detailed Description
Hip fractures are the most frequent and most severe fractures among seniors age 75 and older and they have severe consequences: After a hip fracture, 50% of older persons have permanent functional disabilities, 15-30% require long-term nursing home care, and 10-20% die within one year. Besides the personal burden, hip fractures account for substantial increasing health care expenses. Given the high prevalence, severity and cost of hip fractures, novel care concepts such as STARK are urgently needed to support functionality and autonomy of hip fracture patients - especially in for the first year after the fracture The STARK Intervention is a new care concept for hip fracture patients, which was developed based on prior evidence from clinical trials performed at the Centre on Aging and Mobility at the University of Zurich and important interdisciplinary clinical expertise collected at the Geriatric Trauma Centre at the University Hospital Zurich, the Spitex Zürich, the Dept. of Geriatrics at the University Hospital Zurich, and the Federal Department of Health at the City of Zurich (Gesundheits- und Umweltsdepartement). The aim of the STARK intervention is to enable hip fracture patient to return to their home directly after discharge from acute care by providing a high-quality care concept provided by an interdisciplinary team bridging acute Geriatric Care at the University Hospital and Spitex services (ambulant nursing service at home). With this pilot study, the investigators want to test if the STARK comprehensive autonomy care package improves lower extremity function in the first year after a hip fracture compared to standard of care. Most important secondary outcomes are rate of falls, health care utilization, re-hospitalization and nursing home admission, as well as quality of life, cognitive function, bone mineral density and muscle mass in senior hip fracture patients. This study will include 20 community-dwelling men and women aged 70+ who are hospitalized at the University Hospital Zurich or City Hospital Waid due to an acute hip or pelvis fracture and who are not capable to return home without help. This is a randomized controlled pilot trial with two parallel groups including a control group receiving standard of care (inpatient rehabilitation or home-based or inpatient transitional nursing care) and an intervention group receiving the STARK comprehensive autonomy health care package. The STARK comprehensive autonomy health care package consists on one hand of the STARK-Spitex who will support the participants during the first three months at home and on the other hand of a secondary prevention program including home exercise (3x/week), protein enriched food preparation (20 g whey protein/day), motivation and recommendation for vitamin D supplementation(2000 IE/day), calcium intake and physical activity. The intervention starts already during acute care and involves a multidisciplinary team of geriatricians, nurses and Spitex who assess the care and utilities needs of the patient. Each study participant will undergo 5 clinical visits (at baseline, after 6 weeks, 3 months, 6 months, and 12 months). Between clinical visits, participants will be contacted by phone every month. The STARK comprehensive autonomy health care package can contribute to a faster and sustainable recovery of autonomy after a hip fracture in seniors and might help to lower direct and indirect health care costs by reducing the number of re-hospitalization due to fall-associated injuries.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis, Frailty, Hip Fractures
Keywords
Autonomy, Rehabilitation, Falls, Quality of life, Senior

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
5 (Actual)

8. Arms, Groups, and Interventions

Arm Title
STARK intervention
Arm Type
Active Comparator
Arm Description
New care concept for hip fracture patients
Arm Title
Standard Care
Arm Type
Other
Arm Description
Swiss standard of care for hip fracture patients
Intervention Type
Other
Intervention Name(s)
STARK intervention
Intervention Description
The STARK Intervention is a new care concept for hip fracture patients that enable hip fracture patient to return to their home directly after discharge from acute care. The STARK comprehensive autonomy health care package includes following services; Multidisciplinary collaboration of geriatricians, nurses and Spitex (ambulant nursing service at home) starting already during acute care Inspection of the environment at the patient's home Care and autonomy support Social life support Secondary prevention strategies: Home exercise program (3x/weeks) Protein enriched food preparation (20g whey protein/day) Support to take vitamin D supplementation (2000 IU/day) Recommendation and support to eat calcium rich foods Motivation to be physically active
Intervention Type
Other
Intervention Name(s)
Standard of Care
Intervention Description
Standard of Care involves inpatient rehabilitation or home-based or inpatient transitional nursing care
Primary Outcome Measure Information:
Title
Lower extremity function
Description
Lower extremity function will be measured by the Short Physical Performance Battery (SPPB)
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Gait speed
Description
Gait speed will be obtained from the SPPB.
Time Frame
12 months
Title
Gait speed
Description
Gait speed will be assessed by a 400 m walk test.
Time Frame
12 months
Title
Grip strength
Description
Hand grip strength will be measured using a Martin Vigorimeter.
Time Frame
12 months
Title
Repeated sit-to-stand
Description
Repeated chair stand test will be obtained from the SPPB.
Time Frame
12 months
Title
Rate of falls
Description
Rate of falls will be assessed by a monthly phone call.
Time Frame
12 months
Title
Health care utilization
Description
Health care utilization will be assessed using the health care utilization questionnaire.
Time Frame
12 months
Title
Number of re-hospitalizations
Description
All hospitalizations will be documented as part of the safety documentation(SAE).
Time Frame
12 months
Title
Number of nursing home admissions
Description
All nursing home admissions will be documented.
Time Frame
12 months
Title
Adherence to preventive strategies
Description
Adherence will be documented by the Spitex staff.
Time Frame
3 months
Title
Adherence to preventive strategies
Description
Adherence will be documented by an adherence questionnaire.
Time Frame
12 months
Title
Quality of life
Description
Quality of life will be assessed by the RAND SF-36 questionnaire.
Time Frame
12 months
Title
Quality of life
Description
Quality of life will be assessed by the EuroQol (EQ-5D-3L) questionnaire.
Time Frame
12 months
Title
Cognitive function
Description
Cognitive function will be assessed by the MoCA.
Time Frame
12 months
Title
Cognitive function
Description
Cognitive function will be assessed by the MMSE.
Time Frame
12 months
Title
Appendicular muscle mass
Description
Appendicular muscle mass will be assessed by dual energy X-ray absorptiometry.
Time Frame
12 months
Title
Bone mineral density
Description
Bone mineral density will be assessed by dual energy X-ray absorptiometry.
Time Frame
12 months
Title
Activities of daily living
Description
Activities of daily living will be assessed by questionnaire (PROMIS-HAQ)
Time Frame
12 months
Other Pre-specified Outcome Measures:
Title
Interaction of family carer with hip-fracture patient and health professionals
Description
The interaction will be assessed by semi-structured interviews with a family carer.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Community-dwelling prior to the hip fracture event Living alone or with a partner/family member Living in the city of Zurich age 70+ Acute hip or pelvis fracture after minimal trauma (resulting from a fall occurring from a standard height and without the involvement of others or a vehicle) Living at home without or with minimal (i.e. no more than 1x/day) support from the Spitex (ambulant nursing service) before the hip fracture Participant is mentally competent (judicious) based on the treating physicians' opinion at the screening visit. Inpatient rehabilitation or inpatient transitional care at a nursing home or ambulatory standard of care The participant understands the study procedures and voluntarily agree to participate in the study and comply with all its procedures by giving written informed consent Exclusion Criteria: Patients who are expected to return home without help (i.e. no more care than Spitex 1x/day or physiotherapy 2x/week needed) directly after acute care are excluded. Conservative treatment of acute hip fracture or surgical treatment that does not allow full weight bearing after surgery Currently under cancer treatment or has active cancer (except for non-melanoma skin cancer) Major visual or hearing impairment (visual and/or hearing aids are allowed) or other serious illness that would preclude participation 24-hour nursing care need as this cannot be offered within the STARK package Mobility impairment that precludes return to own apartment Planned nursing home admission after acute hospital stay Current participation in another clinical trial, or plans of such participation in the next 12 months (corresponding to the study duration) Inability to read and/or speak German to an extent necessary to understand instructions and participate in the study Unwilling to forego any additional vitamin D supplementation (bolus or regular intake).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heike Bischoff-Ferrari, Prof.
Organizational Affiliation
Zentrum Alter und Mobilität
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dept. of Geriatrics and Aging Research, University of Zurich / Geriatric Clinic University Hospital Zurich
City
Zürich
State/Province
ZH
ZIP/Postal Code
8037
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Spitex-SpiTal-Autonomie-Reha-Kraft

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