Effects of a goal-setting coaching intervention using accelerometer guided objective real-time feedback on sedentary behaviour and physical activity in older hip fracture patients: The HIP-MOVE Study

Not Applicable

• Conditions: Hip Fracture; Physical Medicine / Rehabilitation - Physiotherapy; Musculoskeletal - Other muscular and skeletal disorders; Public Health - Health promotion/education; Injuries and Accidents - Fractures

• Registration Number: ACTRN12619001630101
• Lead Sponsor: niversity of Adelaide

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-11-25
• Last Update Posted: 10 December 2019

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

i.aged 65 years and above;
ii.admitted to the orthopaedic ward;
iii.able to converse in English;
iv.mobilising independently (with or without a walking aid) prior to admission;
v.living at home or independent living unit prior to hospitalisation;
vi.able to commence the study within 72 hours of admission.

Exclusion Criteria

i.they are admitted from a nursing home, skilled nursing facility (e.g. Sutherland Court) or hospital;
ii.deemed too unwell to participate by the orthogeriatrician (or registrar);
iii.deemed to require palliation by the orthogeriatrician (or registrar);
iv.deemed unable to provide informed consent by the orthogeriatrician (or registrar).
v.they have footdrop following surgery

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sedentary Behaviour (number of sedentary breaks) measured with ActivPAL[At 10 days post-admission or discharge, whichever comes first and 12-weeks post admission];Feasibility of the intervention measured by recruitment, acceptability, completion, safety, and adherence, which all will be recorded. The number of potential participants who refused to participate in the intervention will be used to assess recruitment. Adherence to the trial will be measured by wear adherence, missing data and participation in activities prescribed by the physiotherapists aimed at meeting goals obtained from ActiGraph feedback. Safety will be evaluated by collecting and comparing the number of adverse events and falls during the intervention to data before the intervention started. [10 days post-admission and 12 weeks post-discharge];Physical Activity (time spent standing/stepping) measured with ActivPAL[10 days post-admission, 3 weeks, 6weeks and 12 weeks post-discharge]

Secondary Outcome Measures

Name	Time	Method
Mobility measured by De Morton Mobility Index (DEMMI) at 12 weeks post-admission[12 weeks post-discharge];total sedentary time and bouts measured with ActivPAL[10 days and 12 weeks post admission];sit to stand transitions measured with ActivPAL[10 days and 12 weeks post-admission<br>];Functional recovery measured with Hip Fracture Functional Recovery Scale (Zuckerman et al. 2000)[measured at admission and 3/6 weeks post admission];Quality of life measured with the EQ5D[12 weeks post admission];Falls measured with the Falls Efficacy Scale [12 weeks post admission];Frailty with Clinical Frailty Scale[10 days post-admission and 3, 6 and 12 weeks post-admission];Domain or activity-specific sedentary time with MOST questionnaire[10 days post-admission and 3, 6 and 12 weeks post-admission];Self-reported physical activity with IPAQ-elderly[10 days post-admission and 3, 6 and 12 weeks post-admission]