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Understanding rheumatoid arthritis sufferers motivations and intentions towards exercise prior and post undertaking a five week exercise trial.

Understanding rheumatoid arthritis sufferers motivations and intentions towards exercise prior and post undertaking a five week exercise trial.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12622000519752
Enrollment
30
Registered
2022-04-01
Start date
2023-07-10
Completion date
2024-03-29
Last updated
2023-05-22

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

Conditions

None listed

Brief summary

Patients with rheumatoid arthritis (RA) have a substantially reduced quality of life owing to debilitating reductions in functional capacity. One of the most effective and potent treatments for addressing these issues is with prescriptions of exercise, as recommended by the American College of Sports Medicine guidelines. Previous research has demonstrated that engagement, mastery and physical activity intention were associated with increases in physical activity in arthritis sufferers. The aim of this pilot prospective trial is to determine the effect of an all-inclusive education, exercise and psychological intervention on motivations and intentions to exercise along with physical function outcomes. Understanding each individuals intentions and then addressing them on an individualised basis by educational psychology in conjunction with an individualised exercise program may elucidate positive changes to a rheumatoid arthritis suffers motivation towards physical activity.

Interventions

Participants will undertake an 8-week intervention that incorporates education, behaviour change and exercise. The aim of this pilot prospective trial is to determine the effect of an all-inclusive education, exercise and psychological intervention on motivations and intentions to exercise along with physical function outcomes in rheumatoid arthritis suffers. Participants will complete an initial 1 h assessment with a psychologist to develop and capture their intentions and motivations towards e

Participants will undertake an 8-week intervention that incorporates education, behaviour change and exercise. The aim of this pilot prospective trial is to determine the effect of an all-inclusive education, exercise and psychological intervention on motivations and intentions to exercise along with physical function outcomes in rheumatoid arthritis suffers. Participants will complete an initial 1 h assessment with a psychologist to develop and capture their intentions and motivations towards exercise. After completing the pre-exercise trial participants will receive individualised counselling (1 h per week for two weeks) from the exercise psychologist to develop psychological skills and enhance their motivational orientation towards taking up exercise to invoke positive health behaviour change. Counselling may be undertaking via telehealth or face to face depending on participant preference utilising a semi-structured presentation. Counselling sessions will target the participants identified barriers, motivations, goals and limitations to exercise identified by their baseline questionnaires. Following this participants will undertake a patient specific exercise test with 5 weeks of individualised and partly supervised exercise training and a final assessment in the following week (fitness and completion of questionnaires). Supervised exercise training will be supervised by an Accredited Exercise Physiologist in groups of five. Participants will exercise at a moderate intensity (measured via Borg scale). Face to face exercise sessions (1 h per week) will be undertaken at the QUT Health Clinics with participants also provided a home program to complete twice weekly (45 min per session). Prescribed exercises will include a mixture of upper body push and pull movements e.g. chest press and seated row, lower limb exercises e.g. leg press and sit to stand, balance exercises and cardiorespiratory activity e.g. walking and cycling. Exercise prescription will follow the recommendations from the American College of Sports Medicine with consideration for the participants individual preferences, barriers and goals. Adherence and compliance to the exercise program will be recorded via exercise logs. Education sessions will be delivered face to face by the accredited exercise physiologist during the same weeks as the exercise sessions (1 h per week for four weeks). Education sessions cover the topics of pain, diet, exercise for rheumatoid arthritis and maintaining healthy behaviours. Finally, the participants will undertake a semi-structured interview (30 mins) on their experiences and thoughts from partaking in the trial. Outcome measures utilised in this study have been selected based on industry relevant practitioner based outcomes, exercise intentions, exercise motivators, patient specific function, activities of daily living and quality of life. All assessments will be undertaken by an Accredited Exercise Physiologist and an Accredited Psychologist will conduct the initial pre-intervention counselling.

Sponsors

Queensland University Technology
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment

Eligibility

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

Inclusion criteria

1) >18 years of age and 2) RA stable with no changes in medication in the last 2 months (small changes up to 5 mg in prednisone are allowed) and 3) located within the Brisbane metropolitan area for access to the Queensland University Technology health clinics and 4) English speaking. All participants will consult with their general medical practitioner prior to inclusion to confirm diagnosis and safety to participate.

Exclusion criteria

1) already undertaking >2 days a week of regular moderate intensity exercise training; 2) no other underlying uncontrolled medical conditions that may limit their participation in an exercise program for example including heart disease (heart failure, clinically significant coronary stenosis and previous myocardial infarction), all forms of cancer (both remission and ongoing), knee and hip replacement, and metabolic disease (Type I and II diabetes) and 3) commencement of a new synthetic disease- or biological modifying drug

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026