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PhysiotherapyCOMBINEDNCT05829096

The COMBINED Study to Integrate Health Behaviour Change for People With a Rotator Cuff Disorder

A study testing The COMBINED approach in people with Physiotherapy and Rotator Cuff Syndrome, run by Julie Bury at 4 sites in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

COMBINED is a pragmatic single-arm feasibility study. The goal of this study is to evaluate the implementation of a physiotherapy-led intervention, The COMBINED approach, to facilitate ongoing refinements, including the strategies for implementation, in readiness for a definitive trial in people with a rotator cuff… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
The COMBINED approach
Could I receive a placebo?
No, everyone receives an active treatment
How many people
25 participants
Where
4 sitesUnited Kingdom
Study dates
3 Jul 2023to 25 Oct 2023
Phase
Interventional
Are there results?
None posted in the registry

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 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • The inclusion criteria for the clinician participants are:
  • A qualified (HCPC registered) physiotherapist involved in the management of patients with a RC disorder at one of the trial sites;
  • Willing to consent to the study procedures, including attending a training workshop, audio-recording of the consultations and audit/feedback on intervention delivery.
  • The inclusion criteria for patient participants are:
  • Adult (aged 18 or over);
  • Diagnosed with a RC disorder as per the diagnostic criteria in the British Elbow and Shoulder Society guidelines (Kulkarni et al., 2015), which includes pain mid-range on abduction movement, pain on resisted tests and no loss of external rotation, along with screening of the neck and ruling out other conditions (e.g., instability/frozen shoulder). This will be confirmed by the site Principal Investigators (PI), specialist HCPC registered physiotherapists;
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  • Able to attend at least one face-to-face physiotherapy consultation. Eligibility will be confirmed via physical examination at this session as per the criteria above;
  • Able to give full informed consent;
  • Willing to consent to the study procedures, including audio-recording of the consultations.

Who cannot join

  • The exclusion criteria for the patient participants are:
  • Significant trauma;
  • Neurological or inflammatory causes of their shoulder pain;
  • Any clinical indications of serious pathology.
  • We will not exclude anyone based upon protected characteristics for example, age and ethnicity. Anyone referred into the physiotherapy department with a RC disorder will be eligible to take part in the study. Measures in place may include support for the consent process, consultation or patient interviews where required, for example, if verbal translation is needed via a hospital interpreter, personal interpreter or telephone translation service.

Trial locations and contacts

4 sites in 1 country.

United Kingdom4 sites
  • Doncaster and Bassetlaw NHS Foundation Trust

    Doncaster, South Yorkshire, DN2 5LT

  • Calderdale and Huddersfield NHS Foundation Trsut

    Halifax, West Yorkshire, HX3 0PW

  • Airedale Foundation Trust

    Keighley, West Yorkshire, BD20 6TD

  • University Hospitals of Leicester

    Leicester, Leicestershire, LE1 5WW

Other trials in United Kingdom

About this study

Official title: COmbining Brief Interventions for Modifiable Health Behaviours withIN a Physiotherapy Consultation for pEople With a Rotator Cuff Disorder: Development and Testing in a Single-arm Feasibility Study

COMBINED is a pragmatic single-arm feasibility study. The goal of this study is to evaluate the implementation of a physiotherapy-led intervention, The COMBINED approach, to facilitate ongoing refinements, including the strategies for implementation, in readiness for a definitive trial in people with a rotator cuff disorder. The main questions it aims to answer are: 1) What are the key domains of behaviour change influencing the implementation of The COMBINED approach among physiotherapists? 2) Can The COMBINED approach be delivered as intended? 3) Are there any refinements required to the intervention components? 4) What is the patient experience of receiving The COMBINED approach in an NHS setting?

Read the detailed description

The COMBINED study is looking at how current treatments can be improved for people with shoulder pain, who have been diagnosed with a rotator cuff (RC) disorder. The RC is a group of muscles and tendons which move and stabilise the shoulder joint, and problems with these muscles and tendons can result in pain and difficulty doing everyday tasks.

Current treatments for RC disorders offer only small to moderate benefits and long-term outcomes can be poor. Lifestyle factors, including smoking, being overweight and physical inactivity are associated with the onset and persistence of RC disorders. These factors are linked to modifiable health behaviours that if patients are supported to change, might help improve their shoulder pain. Despite this evidence, physiotherapists do not routinely integrate health behaviour change approaches as part of the management for RC disorders.

The investigators have designed and tested a new complex intervention, The COMBINED approach, that aims to help patients improve their shoulder pain by identifying and assessing the lifestyle factors associated with the onset and persistence of a RC disorder and, where appropriate, the delivery of a brief behaviour change intervention to address these as part of a management plan, supported by a physiotherapist. The investigators have also developed an implementation toolkit to enable and support physiotherapists to effectively deliver this approach in clinical practice. This has been tested and refined in a small usability study, which has led to an optimised version of The COMBINED approach. The investigators would like to find out if this treatment approach can now be delivered within the NHS and to improve this further before testing it in a definitive randomised controlled trial. The overall aim is to provide better care for people with a RC disorder.

This will be a non-randomised feasibility study with qualitative interviews. The study will be conducted in physiotherapy musculoskeletal services across four NHS sites and expected to last 4-6 months. Chartered physiotherapists working at one of the musculoskeletal physiotherapy services, and patients diagnosed with a RC disorder will be eligible to take part.

Physiotherapist participants would be expected to attend a training workshop, deliver the new treatment approach to patients and complete a survey. Patient participants would be asked to attend up to two treatment sessions for their shoulder pain (~60 mins each) with a qualified physiotherapist. During this treatment session they will be asked some questions about their shoulder pain and other things that could be influencing their shoulder pain, such as if they smoke, their weight and how active they are. Where applicable, the physiotherapist may also measure their height and weight during the consultation. The participants will have an examination of their shoulder. Different treatment options will then be discussed. This will be very similar to what participants would expect in a normal physiotherapy appointment. The treatment sessions will be audio-recorded (with consent), for the purpose of checking what information and treatment was delivered by the physiotherapist in the session. The lead researcher may also request (with consent), to observe one of the treatment sessions. The purpose of this is to identify ways to improve how physiotherapists deliver the new treatment approach.

A selection of patients will be asked to take part in an optional short (up to 20 minutes) telephone interview about their views and experience of the treatment session.

Being tested
The COMBINED approach
Keywords
Rotator cuff, Physiotherapy, Shoulder pain, Lifestyle
Medical subject headings
Shoulder Impingement Syndrome, Shoulder Pain

What participants receive

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

  • The COMBINED approachOther

    1. Patient-level intervention:
    • Assessment of existing lifestyle factors (smoking status, physical activity levels, and weight) that may be relevant to shoulder pain;
    • Brief intervention to support health behaviour change: smoking cessation, increasing physical activity levels and consuming a healthy diet
    • Supporting tools for behaviour change, including an activity workbook for goal-setting and a diary for self-monitoring.
    1. Clinician-level implementation toolkit:
    • Training package including a face-to-face workshop, training manual, recorded role play simulations and an online follow-up training session
    • Additional supporting resources; a step-by-step guide to The COMBINED approach, scripts, patient signposting information to support services and a lay summary infographic to explain the links between the health behaviours and RC disorders to patients
    • Audit and feedback via observations of consultations to address any 'drift' from the intervention delivery as intended
Study groups in NCT05829096
Study groupRoleWhat they receive
Intervention armExperimentalThis is a single arm interventional study. 1. A patient-level intervention, which includes: * An assessment of existing lifestyle factors (smoking status, physical activity levels, and weight) that may be relevant to shoulder pain; * A brief intervention to support health behaviour change with respect to the target behaviours of smoking cessation, increasing physical activity levels and consuming a healthy diet * Supporting tools for behaviour change, including an activity workbook for goal-setting and a diary for self-monitoring (attached). The intervention is to be delivered by physiotherapists, integrated within a routine consultation for people with a RC disorder. 2. A clinician-level implementation toolkit to support the delivery of the clinical intervention, which includes a training package and additional resources e.g. scripts to aid conversations with patients.
Receives: Other: The COMBINED approach

What is being measured

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

  1. To assess a change in the Determinants of Behavior Questionnaire (DIBQ)

    Physiotherapy self-report survey

    Measured: At baseline (0 months) and study completion (expected at 6 months)

  2. Fidelity of intervention delivery (self-report checklist by the physiotherapists) will be reported descriptively

    What intervention components were delivered by the physiotherapists as intended

    Measured: 6 months

  3. Fidelity of intervention delivery (observed through audio-recordings by the research team) will be reported descriptively

    What intervention components were delivered by the physiotherapists as intended

    Measured: 6 months

Secondary outcomes (1)
  1. Number of patients recruited that have one or more of the identified lifestyle factor will be reported descriptively

    Identified lifestyle factors include: Smoker; BMI >25kg/m2; physical activity levels <150/minutes of moderate intensity/week

    Measured: 6 months

Timeline

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

  1. First posted25 Apr 2023
  2. Study start3 Jul 2023
  3. Primary completion25 Oct 2023
  4. Study completion25 Oct 2023

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
Model description
Single arm feasibility study
Masking
None (open label)
Enrolment
25 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05829096
Sponsor's protocol ID
51451
Acronym
COMBINED
Status last verified
Aug 2024
First submitted
21 Mar 2023
Last updated
9 Aug 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be available to other researchers

Questions about this trial

What is this clinical trial studying?

A study testing The COMBINED approach in people with Physiotherapy and Rotator Cuff Syndrome, run by Julie Bury at 4 sites in United Kingdom.

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 9 inclusion and 5 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: finished, as of the sponsor's last update on 9 Aug 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in United Kingdom. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To assess a change in the Determinants of Behavior Questionnaire (DIBQ) (time frame: At baseline (0 months) and study completion (expected at 6 months)). The study lists 3 primary outcomes in all. 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 9 Aug 2024.

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