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Prescribing physical activity for patients with hip fracture during rehabilitation

Determining the maximum tolerable dose of prescribed physical activity for patients with hip fracture in inpatient rehabilitation in terms of safety and feasibility

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12613000828729
Acronym
Nil
Enrollment
30
Registered
2013-07-26
Start date
2013-09-20
Completion date
2013-12-13
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

We already know that the amount of walking completed by people in rehabilitation is very low and people find it hard to regain their walking ability in the community after having a hip fracture. This study will find out how much walking can be feasibly and safely completed by people in rehabilitation after having a hip fracture. The results will help guide therapists as to how much walking they could prescribe to optimise patient outcomes.

Interventions

This is a phase I dose-response trial to find out how much physical activity, in the form of walking, can be prescribed for people with hip fracture during rehabilitation in terms of safety and feasibility. In addition to receiving usual rehabilitation care, groups of 3 participants will be individually supervised to walk at a prescribed level of physical activity for 5 consecutive days. This prescribed level of physical activity will not change for individual participants over the 5 days but m

This is a phase I dose-response trial to find out how much physical activity, in the form of walking, can be prescribed for people with hip fracture during rehabilitation in terms of safety and feasibility. In addition to receiving usual rehabilitation care, groups of 3 participants will be individually supervised to walk at a prescribed level of physical activity for 5 consecutive days. This prescribed level of physical activity will not change for individual participants over the 5 days but may escalate for subsequent groups of participants. The dose level of prescribed physical activity will follow a modified Fibonacci scheme starting with an initial dose of 3 minutes of moderate intensity supervised walking per day for the first group of participants. Moderate intensity walking will be defined as a 3 on the modified Borg 0-10 perceived exertion scale, where 3 = “I am still comfortable but am breathing a little harder.” Dose escalation will depend on the presence or absence of adverse incidents among the group of 3 participants. Depending on the feasibility and safety of the prescribed dose of walking, the dose may or may not be escalated between subsequent groups of participants. Dose escalation will start with early larger dose increments between groups which get smaller for higher doses until the guideline stopping value of 30 minutes of walking per day is reached (i.e. 3, 6, 10, 15, 21, 27, 30 mins). The trial will stop when/if a group of participants can achieve 30 minutes of prescribed walking as this reflects physical activity guidelines.

Sponsors

Nicholas Taylor
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Other
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients will be eligible if they are: - admitted to rehabilitation following surgical management of a hip fracture - receive medical approval to participate - can walk, either independently or with assistance.

Exclusion criteria

Patients will not be eligible to participate if they: - are admitted with diagnoses other than hip fracture - are not able to walk - have moderate to severe cognitive impairment.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026