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The Direct-Physio Trial

Direct Access to Physiotherapy for Acute Low Back Pain: a Pragmatic Pilot Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05215093
Enrollment
200
Registered
2022-01-31
Start date
2022-12-01
Completion date
2026-09-01
Last updated
2026-09-17

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

Conditions

Low Back Pain, Physiotherapy

Keywords

Direct access

Brief summary

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.

Interventions

OTHERDirect access physiotherapy for acute low back pain

Interventions include physiotherapeutic treatment, without prescription of the general practitioner, for low back pain according to current biopsychosocial national (KCE - Belgium) and international (NICE) guidelines.

OTHERUsual care for acute low back pain

Interventions include standard of care by the general practitioner for low back pain according to current biopsychosocial national (KCE - Belgium) and international (NICE) guidelines.

Sponsors

Hasselt University
Lead SponsorOTHER
KU Leuven
CollaboratorOTHER
Universiteit Antwerpen
CollaboratorOTHER
Université Catholique de Louvain
CollaboratorOTHER
Axxon - the Belgian physiotherapy professional association
CollaboratorUNKNOWN
Riziv-Inami - National Institute for the Sickness and Invalidity Insurance
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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).

Design outcomes

Primary

MeasureTime frameDescription
Changes in pain intensityImmediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollmentNumeric Rating Scale
Changes in pain location and extentImmediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollmentPain Diagram of Margolis
Changes in disabilityImmediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollmentOswestry Disability Index

Secondary

MeasureTime frameDescription
Cost-effectiveness of the provided treatment (direct physiotherapy access vs usual care for acute low back pain)Up to 2 years after enrollmentCosts of low back pain and its treatment in terms of medical and societal costs
Changes in beliefs and cognitions related to low backImmediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollmentBack Pain Attitude Questionnaire (Back-PAQ)
Changes in patient satisfactionImmediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollment
Changes in quality of lifeImmediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollmentEQ-5D
Amount of / coping with flare-ups during follow-upImmediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollment

Countries

Belgium

Contacts

PRINCIPAL_INVESTIGATORLotte Janssens, PhD

UHasselt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026