search
Back to results

The Direct-Physio Trial

Primary Purpose

Low Back Pain, Physiotherapy

Status
Recruiting
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Direct access physiotherapy for acute low back pain
Usual care for acute low back pain
Sponsored by
Hasselt University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Low Back Pain focused on measuring Direct access

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept 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).

Sites / Locations

  • REVAL Faculty of Rehabilitation SciencesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Direct physiotherapy pathway

Usual care pathway

Arm Description

People with acute low back pain will directly go to a physiotherapist, who will treat the patient without prescription of the general practitioner.

People with low back pain will receive usual care by the general practitioner (with or without referral to physiotherapy).

Outcomes

Primary Outcome Measures

Changes in pain intensity
Numeric Rating Scale
Changes in pain location and extent
Pain Diagram of Margolis
Changes in disability
Oswestry Disability Index

Secondary Outcome Measures

Cost-effectiveness of the provided treatment (direct physiotherapy access vs usual care for acute low back pain)
Costs of low back pain and its treatment in terms of medical and societal costs
Changes in beliefs and cognitions related to low back
Back Pain Attitude Questionnaire (Back-PAQ)
Changes in patient satisfaction
Changes in quality of life
EQ-5D
Amount of / coping with flare-ups during follow-up

Full Information

First Posted
December 13, 2021
Last Updated
February 27, 2023
Sponsor
Hasselt University
Collaborators
KU Leuven, Universiteit Antwerpen, Université Catholique de Louvain, Axxon - the Belgian physiotherapy professional association, Riziv-Inami - National Institute for the Sickness and Invalidity Insurance
search

1. Study Identification

Unique Protocol Identification Number
NCT05215093
Brief Title
The Direct-Physio Trial
Official Title
Direct Access to Physiotherapy for Acute Low Back Pain: a Pragmatic Pilot Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 1, 2022 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hasselt University
Collaborators
KU Leuven, Universiteit Antwerpen, Université Catholique de Louvain, Axxon - the Belgian physiotherapy professional association, Riziv-Inami - National Institute for the Sickness and Invalidity Insurance

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain, Physiotherapy
Keywords
Direct access

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Direct physiotherapy pathway
Arm Type
Experimental
Arm Description
People with acute low back pain will directly go to a physiotherapist, who will treat the patient without prescription of the general practitioner.
Arm Title
Usual care pathway
Arm Type
Active Comparator
Arm Description
People with low back pain will receive usual care by the general practitioner (with or without referral to physiotherapy).
Intervention Type
Other
Intervention Name(s)
Direct access physiotherapy for acute low back pain
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
Usual care for acute low back pain
Intervention Description
Interventions include standard of care by the general practitioner for low back pain according to current biopsychosocial national (KCE - Belgium) and international (NICE) guidelines.
Primary Outcome Measure Information:
Title
Changes in pain intensity
Description
Numeric Rating Scale
Time Frame
Immediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollment
Title
Changes in pain location and extent
Description
Pain Diagram of Margolis
Time Frame
Immediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollment
Title
Changes in disability
Description
Oswestry Disability Index
Time Frame
Immediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollment
Secondary Outcome Measure Information:
Title
Cost-effectiveness of the provided treatment (direct physiotherapy access vs usual care for acute low back pain)
Description
Costs of low back pain and its treatment in terms of medical and societal costs
Time Frame
Up to 2 years after enrollment
Title
Changes in beliefs and cognitions related to low back
Description
Back Pain Attitude Questionnaire (Back-PAQ)
Time Frame
Immediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollment
Title
Changes in patient satisfaction
Time Frame
Immediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollment
Title
Changes in quality of life
Description
EQ-5D
Time Frame
Immediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollment
Title
Amount of / coping with flare-ups during follow-up
Time Frame
Immediately before, during the first 6 weeks and immediately after intervention and at 3 months, 1 and 2 years after enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pieter Severijns, PhD
Phone
+32477560517
Email
pieter.severijns@uhasselt.be
First Name & Middle Initial & Last Name or Official Title & Degree
Lotte Janssens, PhD
Email
lotte.janssens@uhasselt.be
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lotte Janssens, PhD
Organizational Affiliation
UHasselt
Official's Role
Principal Investigator
Facility Information:
Facility Name
REVAL Faculty of Rehabilitation Sciences
City
Diepenbeek
ZIP/Postal Code
3590
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pieter Severijns
Email
pieter.severijns@uhasselt.be

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

The Direct-Physio Trial

We'll reach out to this number within 24 hrs