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Effect of a digital intervention on pain and reliance on opioids after total knee replacement surgery

Evaluating the implementation and effectiveness of a digital intervention on pain and reliance on opioids after total knee replacement surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624001060538
Enrollment
4
Registered
2024-09-03
Start date
2025-05-22
Completion date
2026-06-22
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

The efficacy and safety of digitally delivered pain self-management interventions for reducing pain after surgeries, including total knee replacement (TKR), have been demonstrated in several randomised controlled trials. However, little is known about the feasibility and effectiveness of these interventions in Australian hospital settings. The current project evaluates the implementation and effectiveness of an mHealth intervention designed to support patients’ engagement with pain self-management after TKR surgery. Consenting patients (N = 130) who are scheduled to undergo TKR surgery will be randomised to receive either a psychoeducational video prior to surgery, and one SMS text message per day for 3 weeks after surgery, or the pre-surgery psychoeducational video only. Both groups will continue to receive usual care. Outcome measures including pain intensity (primary), opioid dose, pain-related distress, and perceived social isolation will be recorded at baseline, 3 days, 3 weeks, 6 weeks, 3 months, and 6 months after surgery using self-reported surveys. Pain self-efficacy will be measured at 6 week, 3 months and 6 months post-surgery. Implementation outcomes will be evaluated using mixed (quantitative-qualitative) methods. This trial represents a first step towards the translation of digitally delivered non-pharmacological acute pain management in the Australian healthcare system.

Interventions

Up to one week prior to their scheduled surgery date, participants in the intervention group will receive a short (10 minute) psychoeducational video (via text message containing a hyperlink) addressing patients confidence and motivation to use non-pharmacological pain self-management strategies (e.g. physical activity, pacing, social engagement) to manage pain in combination with prescribed medications. Each day after surgery for three weeks, participants will then receive one text message (bet

Up to one week prior to their scheduled surgery date, participants in the intervention group will receive a short (10 minute) psychoeducational video (via text message containing a hyperlink) addressing patients confidence and motivation to use non-pharmacological pain self-management strategies (e.g. physical activity, pacing, social engagement) to manage pain in combination with prescribed medications. Each day after surgery for three weeks, participants will then receive one text message (between 160 to 320 characters) providing them with reassurance (validation, encouragement, support) and reminders about pain and how to effectively manage pain by using pain self-management strategies. The messages serve to reinforce the material in the psychoeducational video. Adherence to the intervention (watching the video, reading text messages) will be self-reported by patients in a survey at the end of the trial.

Sponsors

Austin Health
Lead SponsorHospital

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

- patients who are scheduled for Total Knee Replacement (TKR) surgery - own a mobile phone with access to the internet - capable of watching a 10-minute video with audio and subtitles, receiving, reading, and understanding short SMS text messages - capable in completing brief online surveys - able to provide independent consent to participate

Exclusion criteria

- cognitive impairment, visual impairment, or a mental health condition affecting their ability to provide independent consent or affecting their ability to understand and complete survey measures - difficulty reading or understanding English

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026