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Clinical Trials/NCT01930409
NCT01930409
Completed
Not Applicable

A Feasibility Study Investigating Telephone Supported Discharge From Acute Care to the Community After Hip Fracture

University of British Columbia1 site in 1 country30 target enrollmentNovember 2013
ConditionsHip Fracture

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hip Fracture
Sponsor
University of British Columbia
Enrollment
30
Locations
1
Primary Endpoint
Feasibility of study recruitment and retention
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to determine whether is is feasible and acceptable to deliver a telephone based coaching intervention compared with education alone in community dwelling older adults (age 60 and older) after a fall related hip fracture.

Detailed Description

The investigators propose a randomized controlled trial design to inform the development of a larger scale study to test effectiveness of a clinician supported telephonic self management intervention for older adults after hip fracture. The primary aim is to determine feasibility and acceptability of the intervention, and the secondary aim is to measure statistical trends on quality of life at 4 months after fracture in community dwelling older adults. In parallel, we will conduct a process evaluation to ascertain key features of the intervention via qualitative interviews of participants and health care professionals involved in delivery of the intervention.

Registry
clinicaltrials.gov
Start Date
November 2013
End Date
January 2015
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dolores Langford

Principal Investigator

University of British Columbia

Eligibility Criteria

Inclusion Criteria

  • Adults (men and women) over 60 years of age
  • Fall related hip fracture
  • Community dwelling
  • English speaking

Exclusion Criteria

  • Medical co-morbidities precluding physical activity (significant heart failure, palliative conditions etc.)
  • Profound hearing loss

Outcomes

Primary Outcomes

Feasibility of study recruitment and retention

Time Frame: 1 year

Feasibility will be measured by recruitment rate (30%), and retention rate (\<10% attrition)

Secondary Outcomes

  • Quality of Life EQ5D-5L(4 months)

Study Sites (1)

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