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The Direct-Physio Trial

H

Hasselt University

Status

Enrolling

Conditions

Physiotherapy
Low Back Pain

Treatments

Other: Direct access physiotherapy for acute low back pain
Other: Usual care for acute low back pain

Study type

Interventional

Funder types

Other

Identifiers

NCT05215093
CME2021/066

Details and patient eligibility

About

Previous research showed that direct access to physiotherapy, and the associated early physiotherapeutic treatment of patients with low back pain (LBP), results in improved clinical outcomes, as well as reduced health-related costs. However, despite these results, the effectiveness of direct access to physiotherapy and its impact on costs has never been investigated in Belgium. Therefore, the goal of this study is to compare the (cost-)effectiveness of direct access to physiotherapy compared to usual care by the general practitioner (GP) for patients with acute LBP.

In this study, 600 patients with acute LBP (lasting >24 hours and <6 weeks) will be divided into two groups (Dutch-speaking: n=2x150; French-speaking n= 2x150). One group will receive treatment through direct access to the physiotherapist, without prescription by a GP. The other group will follow the traditional care pathway through the GP. Th effects on pain, disability and cost-effectiveness will be analysed using questionnaires obtained before and at the end of treatment, after 3 months, after one and after two years. Primary outcomes include pain and disability. Secondary outcomes include clinical outcomes, beliefs related to LBP, quality of life, patient satisfaction, but also direct health care costs, health care resource use, as well as absenteeism and productivity loss.

The results of this study will answer the question whether direct access to physiotherapy is (cost)effective for acute LBP. In the long term, these results might be used to optimize the care pathway in Belgium for patients with acute low back pain.

Enrollment

600 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with non-specific acute LBP defined as (based on Nicol et al. 2020):

    • pain between the 12th rib and buttocks
    • associated or not with non-dominant leg pain
  • looking for LBP care for the first time in case of first episode, OR for the first time for the current episode in case of recurrent or persistent LBP

  • lasting > 24 hours and < 6 weeks

  • with an average pain intensity during the past 24 hours of ≥ 3 on an 11-point Numerical Pain Rating Scale

  • with an Oswestry Disability Index score (version 2.1a) of at least 20% (Denteneer et al. 2018).

  • Patients aged between 18 and 65 years

Exclusion criteria

  • Recent lumbar surgery (< 1 year)
  • Pregnancy
  • History of (any) treatment for the current pain episode
  • Red flags suggesting specific LBP (e.g. resulting from infection or neoplasm, cauda equina), based on the Belgian Health Care Knowledge Center (KCE, BEL) who published evidence-based guidelines to manage LBP and radicular pain (Van Wambeke et al. 2017), leads to exclusion from treatment within the study.
  • Generalized musculoskeletal pain (based on fibromyalgia criteria) (Galvez-Sánchez and Reyes del Paso 2020).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

600 participants in 2 patient groups

Direct physiotherapy pathway
Experimental group
Description:
People with acute low back pain will directly go to a physiotherapist, who will treat the patient without prescription of the general practitioner.
Treatment:
Other: Direct access physiotherapy for acute low back pain
Usual care pathway
Active Comparator group
Description:
People with low back pain will receive usual care by the general practitioner (with or without referral to physiotherapy).
Treatment:
Other: Usual care for acute low back pain

Trial contacts and locations

1

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Central trial contact

Pieter Severijns, PhD; Lotte Janssens, PhD

Data sourced from clinicaltrials.gov

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