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Efficacy of a digital pain management intervention on pain and reliance on opioids in patients with rib fractures

Evaluating the efficacy of a digital behavioural pain management intervention to improve analgesia and reduce reliance on opioids in adult patients with rib fractures

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12623000006640
Enrollment
5
Registered
2023-01-09
Start date
2024-05-31
Completion date
2025-07-01
Last updated
2025-09-08

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

Conditions

None listed

Brief summary

Patients who engage with behavioural pain management strategies (e.g., relaxation, thought management) have better pain relief and use less opioids. However, delivering these strategies in hospital settings can be costly and often is not feasible during acute pain service rounds. Emerging research indicates that behavioural pain management education can effectively be delivered using low-cost digital technology. The aim of this study is to test the hypothesis that patients who receive an mHealth intervention (educational video + supportive daily text messages) will utilise lower doses of opioids across the first week of hospitalisation and one week after discharge compared to those who receive the education video only.

Interventions

Digital behavioural pain management - Delivered entirely via one-way SMS (text messaging) - Patients will initially be sent an SMS with a link to an online video resource containing brief, evidence based, behavioural pain management education (BPME). The video will be approximately 10 minutes in duration and will include narrated, animated PowerPoint slides with information on behavioural pain management strategies (e.g., relaxation techniques and distraction) as well as education about rib frac

Digital behavioural pain management - Delivered entirely via one-way SMS (text messaging) - Patients will initially be sent an SMS with a link to an online video resource containing brief, evidence based, behavioural pain management education (BPME). The video will be approximately 10 minutes in duration and will include narrated, animated PowerPoint slides with information on behavioural pain management strategies (e.g., relaxation techniques and distraction) as well as education about rib fractures (e.g., timeline of recovery). Patients will then receive two SMS per day (mid-morning and mid-afternoon) for 14 consecutive days (encompassing up to a week of hospitalisation and one-week post-discharge). Text messages serve to remind patients about the information provided in the behavioural pain management educational video (e.g., “If you inhale deeply, your lungs will stay healthy and reduce your chance of an infection”) and reassure patients that pain after rib fractures is normal (“Rib fractures are surprisingly common and can really hurt. Hang in there though! It will hurt less and less every day as your body heals”). - Intervention will be co-designed with patients who have recently been in hospital with rib fractures and clinicians experienced in managing rib fractures. Patients and clinicians will be presented with the online video resource and example text messages and invited to provide feedback on appropriateness and usefulness/helpfulness. The content of the video and text messages will be adjusted in response to the feedback. - Intervention will be received in addition to usual care. Usual care in this context is multidisciplinary with a focus on maximising non-opioid analgesia while encouraging pulmonary hygiene. It may include incentive spirometry, high flow nasal prong oxygen, and/or multimodal analgesia (including patient-controlled analgesia). - Engagement with the video will be assessed using a study-specific questionnaire shortly after participants receive the link to the video. Participants will asked to confirm they have watched the video by answering two questions about the content of the video. - Engagement with the text messages will be assessed using a using a study-specific questionnaire at the end of the study. Participants in the intervention group will be asked whether or not they read the text messages they were sent during the study.

Sponsors

Northern Sydney Local Health District
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

- Age 18 years or older - With isolated rib fracture/s - Within one day of hospital admission - Able to understand written and spoken English. - Owns a mobile phone that receives text messages - Able to give written informed consent and comply with study procedures

Exclusion criteria

- Inability to complete study procedures (lack of fluency in English, cognitive ability, mental health status, medical status) - Admission to hospital with other injuries or comorbidities (e.g., head, extremity, lung, or abdominal trauma) - NSAIDs contraindicated - Regional anaesthesia or blockade likely to be used for pain management

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 5, 2026