AzTrials
AzTrials

Collaborative Clinical ReasoningNCT07802951

Collaborative Clinical Reasoning: Perceptions and Practices of General Practitioners, Physical Therapists, and Patients With Low Back Pain in Primary Care

A study testing Focus groups and deliberative workshop in people with Collaborative Clinical Reasoning, run by Université Catholique de Louvain at 1 site in Belgium.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

Low back pain is a major health problem in primary care and is associated with a substantial clinical, economic, and societal burden. Although evidence-based recommendations are available, its management remains heterogeneous, poorly coordinated, and often characterized by overmedicalization. Read more about this study

Who is it for?
Ages 18 to 100 years
Conditions the study is for
Collaborative Clinical Reasoning
What is being tested?
Focus groups and deliberative workshop
Could I receive a placebo?
No, everyone receives an active treatment
How many people
225 participants
Where
1 siteBelgium
Study dates
Sep 2026to Dec 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 100 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • General Practitioners
  • Be a general practitioner or a physician in postgraduate training in general practice.
  • Practice general medicine in French-speaking Belgium.
  • Practice general medicine in primary care.
  • Physiotherapists
  • Be a physiotherapist.
Show all 12Show fewer
  • Practice physiotherapy in French-speaking Belgium.
  • Practice physiotherapy in primary care.
  • Patients with low back pain
  • Age ≥18 years.
  • Have low back pain (pain between the lower margin of the ribs and the gluteal fold, with or without pain in one or both legs).
  • Have consulted both a general practitioner and a physiotherapist for this condition in primary care in French-speaking Belgium.

Who cannot join

  • General Practitioners
  • 1. Be on sick leave during the study (e.g., work incapacity)
  • Physiotherapists
  • Practice exclusively in a nursing home or a nursing home with skilled nursing care.
  • Be on sick leave during the study (e.g., work incapacity).
  • Patients with low back pain
Show all 11Show fewer
  • Have a known specific lumbar pathology (e.g., fracture, infection, cancer, lumbar radiculopathy, etc).
  • Have a known general condition that may explain the low back pain (e.g., fibromyalgia, osteoporosis, rheumatologic disease, etc).
  • Have undergone back surgery within the past 12 months.
  • Be pregnant or have had a known pregnancy within the past 12 months.
  • Reside in a nursing home or a nursing home with skilled nursing care.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Olivier Hunin, PT, Msc contact

+32478836693

olivier.hunin@uclouvain.be

Franck Verschuren, MD, PhD contact

+32486120571

franck.verschuren@uclouvain.be

Belgium1 site, 1 recruiting
  • UCLouvain - Institute of Health and Society (IRSS)

    Woluwe-Saint-Lambert, Brussels Capital, 1200

    Olivier Hunin, PT, Msc, +32478836693, olivier.hunin@uclouvain.be

    Franck Verschuren, MD, PhD, +32486120571, franck.verschuren@uclouvain.be

    Recruiting

Other trials in Belgium

About this study

Low back pain is a major health problem in primary care and is associated with a substantial clinical, economic, and societal burden. Although evidence-based recommendations are available, its management remains heterogeneous, poorly coordinated, and often characterized by overmedicalization. In this context, interprofessional collaboration has been identified as a means of improving primary care but does not necessarily ensure a shared understanding of clinical situations. Collaborative Clinical Reasoning (CCR), defined as the process of developing a shared mental model among healthcare professionals and patient partners, remains insufficiently explored in primary care.

This exploratory qualitative study aims to explore the representations and definitions of Collaborative Clinical Reasoning among general practitioners, physiotherapists, and patient partners with low back pain in French-speaking Belgium. It also aims to examine how CCR is implemented in primary care practice and to identify perceived barriers and facilitators to its implementation.

Data will be collected through separate focus groups involving general practitioners, physiotherapists, and patient partners with low back pain. Qualitative data will be analyzed using inductive reflexive thematic analysis.

Being tested
Focus groups and deliberative workshop
Keywords
Collaborative Clinical Reasoning, Interprofessional collaboration, Low Back Pain, Primary Care
Medical subject headings
Low Back Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Focus groups and deliberative workshopOther

    General practitioners, physiotherapists, and patients will first participate in separate focus groups for each stakeholder group. A subsequent mixed deliberative workshop will bring together participants from the three stakeholder groups to discuss and refine the findings.

Study groups in NCT07802951
Study groupRoleWhat they receive
General Practitioners, Physiotherapists, and Patients with non-specific low backOtherNot described
Receives: Other: Focus groups and deliberative workshop

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Participants' representations and definitions of Collaborative Clinical Reasoning, identified through reflexive thematic analysis.

    Participants' representations and definitions of Collaborative Clinical Reasoning will be explored through qualitative data collected during separate focus groups with general practitioners, physiotherapists, and patients with non-specific low back pain, as well as during a subsequent deliberative workshop bringing together these three participant groups.

    Measured: From the initial focus groups to the subsequent deliberative workshop, over an estimated 15-month data collection period.

Secondary outcomes (2)
  1. Enactment of Collaborative Clinical Reasoning in primary care practice, identified through reflexive thematic analysis.

    The enactment of Collaborative Clinical Reasoning in primary care practice will be explored through qualitative data collected during separate focus groups with general practitioners, physiotherapists, and patients with non-specific low back pain, as well as during a subsequent deliberative workshop bringing together these three participant groups.

    Measured: From the initial focus groups to the subsequent deliberative workshop, over an estimated 15-month data collection period.

  2. Barriers and facilitators to the enactment of Collaborative Clinical Reasoning in primary care practice, identified through reflexive thematic analysis.

    Barriers and facilitators influencing the enactment of Collaborative Clinical Reasoning in primary care practice will be explored through qualitative data collected during separate focus groups with general practitioners, physiotherapists, and patients with non-specific low back pain, as well as during a subsequent deliberative workshop bringing together these three participant groups.

    Measured: From the initial focus groups to the subsequent deliberative workshop, over an estimated 15-month data collection period.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Sep 2026
  2. Study startSep 2026 (estimated)
  3. Primary completionDec 2027 (estimated)
  4. Study completionDec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
225 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07802951
Sponsor's protocol ID
RCC
Status last verified
Sep 2026
First submitted
24 Aug 2026
Last updated
10 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Focus groups and deliberative workshop in people with Collaborative Clinical Reasoning, run by Université Catholique de Louvain at 1 site in Belgium.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 12 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 10 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Olivier Hunin, PT, Msc (+32478836693, olivier.hunin@uclouvain.be), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Participants' representations and definitions of Collaborative Clinical Reasoning, identified through reflexive thematic analysis. (time frame: From the initial focus groups to the subsequent deliberative workshop, over an estimated 15-month data collection period.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Sep 2026.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in