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Back to the Future: Bridging the Hospital to Home Continuum After Hip Fracture

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01930409
Acronym
B2F
Enrollment
30
Registered
2013-08-28
Start date
2013-11-30
Completion date
2015-01-31
Last updated
2017-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Fracture

Keywords

Femoral Fractures, Hip Fractures, Frail older adults, Quality of Life, Feasibility Studies

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.

Interventions

BEHAVIORALTelephone Support and Coaching

The participants will receive up to 5 telephone calls of 30-45 minutes each after hospital discharge to provide support and education for the transition from acute to community care. The first call will be made within 48-72 hours of hospital discharge and will have the following elements: * Health Status * Medication Management * Activity/Exercise Prescription and Goal-Setting * Falls Prevention * Clarification of Appointments * Coordination of Post-Discharge Home Services * What To Do If a Problem Arises

BEHAVIORALEducation Only

An educational toolkit will be provided, with materials to self manage at home after hospital discharge following a fall related hip fracture

Sponsors

University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of study recruitment and retention1 yearFeasibility will be measured by recruitment rate (30%), and retention rate (\<10% attrition)

Secondary

MeasureTime frameDescription
Quality of Life EQ5D-5L4 monthsThe EQ5D-5L Quality of Life outcome measure is a self reported questionnaire measure, and has been extensively investigated in the hip fracture population, with well established sensitivity, reliability and validity properties.

Other

MeasureTime frameDescription
Gait (Walking) speed4 monthsGait speed is a reliable, valid and sensitive measure likened to a vital sign.
Falls FES-14 monthsFalls self efficacy questionnaire will be used.
Quality of Life ICECAP-O4 months
Falls self report diary4 monthsParticipants will record Falls in a check box format daily
The Hospital Anxiety and Depression Scale (HADS)4 monthsThe HADS is a 14 item self reported questionnaire designed to assess anxiety and depression
Pain: Visual Analogue Scale (VAS)4 months
de Morton Mobility Index (DEMMI)4 monthsThe DEMMI is a clinical instrument for measuring mobility in older adults. Interval levels are obtained from 0 (poor mobility) to 100 (excellent mobility)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026