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An evaluation of the Flinders Program to improve patient quality of life and self-management competencies in osteoarthritis and co-occurring obesity: A randomised controlled trial.

A randomised controlled trial evaluating the impacts of the self-management support Flinders Program on Health Related Quality of Life of obese osteoarthritis patients on a knee or hip replacement waiting list

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000674538
Enrollment
94
Registered
2015-06-29
Start date
2015-07-07
Completion date
Unknown
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

Does the Flinders self-management support program improve HRQoL for obese osteoarthritis patients on a total knee or hip arthroplasty waiting list? Does the self-management support Flinders program help obese osteoarthritis patients on a total knee or hip arthroplasty waiting list to reduce their obesity? What demographic and psychosocial factors contribute to weight loss for obese osteoarthritis patients on a total knee or hip arthroplasty waiting list?

Interventions

The intervention group will receive the self-management support Flinder Program for six months. Flinders Program is a one-to-one self-management support program. It involves a 1-hour face-to-face session during which a trained nurse and the participant identify and prioritise the issues due to the chronic condition(s) the participant has. They then agree on a care plan based upon goals established for prioritised issues. Adherence to the intervention is monitored by weekly/fortnightly (based on

The intervention group will receive the self-management support Flinder Program for six months. Flinders Program is a one-to-one self-management support program. It involves a 1-hour face-to-face session during which a trained nurse and the participant identify and prioritise the issues due to the chronic condition(s) the participant has. They then agree on a care plan based upon goals established for prioritised issues. Adherence to the intervention is monitored by weekly/fortnightly (based on a mutual agreement) phone calls.

Sponsors

International Musculoskeletal Research Institute
Lead SponsorOther

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

1-Indicated for a primary total knee or hip arthroplasty due to osteoarthritis 2-have a BMI of 30 kg/m2 or above 3-willingly provide signed informed consent form to participate in the study

Exclusion criteria

1-cannot or will not provide signed informed consent for participation in the study. 2-have an emotional or neurological condition that would pre-empt their ability or willingness to participate in the study including mental illness, intellectual disability, drug or alcohol abuse. 3-have had a surgery within the last three months 4-have dementia 5-Patients who have a pacemaker or ICD will be excluded from the bio-impedance test.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026