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Evaluate the feasibility and effectiveness of a pilot chronic low back program for Ezidi refugees: a waitlist-controlled study

Evaluate the feasibility and effectiveness of a pilot chronic low back program for Ezidi refugees: a waitlist-controlled study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624001386527
Enrollment
17
Registered
2024-11-22
Start date
2021-07-05
Completion date
2022-01-28
Last updated
2024-12-02

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

Conditions

None listed

Brief summary

Armidale was selected for the settlement of Ezidi refugees as part of Australia’s humanitarian resettlement program. Approximately, 600 refugees settled in Armidale from February 2018. One of the most frequently presented health conditions is chronic low back pain. Chronic low back pain was the reason for 62% of total referrals to the physiotherapy service of Armidale Rural Referral Hospital. Therefore, it was decided that a group program was needed to meet this need. The program was offered to any Ezidi patients with chronic low back pain. The duration of the program is for 8 weeks. The program included exercise classes and education sessions. This program ran for a 6 month period time. At the end of the 6 month period, an evaluation of the program will take place to assess benefit of continuation of the program and necessary modifications. There have been no previously reported studies evaluating the effectiveness of a group program for refugee populations with chronic low back pain. This study aims to assess the acceptance and effectiveness of such a group program.

Interventions

The group program included 1x weekly 30-minutes education sessions tailored for delivery using methods appropriate to the low level of health literacy of the participants, 2x weekly 1-hour exercise classes and 1 x weekly home exercise. This program was a multi-disciplinary intervention. The education sessions included introduction to the program; information about aerobic, progressive strengthening and motor control exercises; pain; pain and physical activity; pain and pacing; chronic pain and m

The group program included 1x weekly 30-minutes education sessions tailored for delivery using methods appropriate to the low level of health literacy of the participants, 2x weekly 1-hour exercise classes and 1 x weekly home exercise. This program was a multi-disciplinary intervention. The education sessions included introduction to the program; information about aerobic, progressive strengthening and motor control exercises; pain; pain and physical activity; pain and pacing; chronic pain and medication; psychology in chronic pain; and nutrition and chronic pain. The education sessions were delivered by a physiotherapist, a dietitian, a pharmacist and a psychologist. The exercise program included 20 minutes of high intensity aerobic, progressive strengthening and motor control exercises. The exercise program included 20 minutes of high intensity aerobic, progressive strengthening and motor control exercises. The aerobic exercises were either treadmill or stationary bike training with the aim of achieving 50% to 85% of the individual’s age-predicted maximal heart rate. The strengthening exercises were with upper and oblique abdominals from the supine position with knees bent, lower abdominal crunches, full abdominal crunches, lifting trunk to neutral from prone position and arms in elevation, straight leg lifts toward ceiling and bridging with the exercise intensity progressed from 2 sets of 10 repetitions (weeks 1–2), 2 sets of 15 repetitions (weeks 3–4) to 3 sets of 10 repetitions (weeks 5–6) and 3 sets of 15 repetitions (weeks 7–8). For the motor control exercises, the participants were trained how to activate their transversus abdominus muscles which was facilitated by visualization techniques, verbal instruction, manual palpation and education using illustrations. Participants were instructed to complete controlled, low-level contractions, rather than maximum strength contractions. Training commenced in a low-load non-functional position (prone lying, four-point kneeling, supine lying with flexed knees). Holding time for exercises was gradually increased. Once the participants were able to perform sustained contractions in low-load postures, the exercises were progressed to functional tasks such as lifting an object, pushing a trolley, cleaning the floor, vacuuming, washing dishes and folding laundry. The exercise classes were supervised by a physiotherapist with groups of 6 participants. The total duration was 8 weeks. Assessing and monitoring was carried out by the physiotherapist at the class, and participants' attendance were recorded with a checklist for each exercise. All participants had 8 weeks of waiting time(control) and all participants participated in the intervention(Intervention).

Sponsors

Hunter New England Health
Lead SponsorGovernment body

Study design

Allocation
Non-randomised trial
Primary purpose
Treatment

Eligibility

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

Inclusion criteria

A convenience sample of all Ezidi refugee patients aged 18 years or over, referred to physiotherapy for management chronic low back pain, were invited to participate in the program.

Exclusion criteria

Any patients who had muscle strength less than 3/5 on manual muscle testing or cauda equina syndrome were excluded from the study.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026