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Distraction Techniques for Postoperative Pain After Total Knee Arthroplasty: A Randomized Controlled Trial

he Effect of Virtual Reality Headset, Squishy (Squeeze Toy), and Poetry Reading on Postoperative Pain Control After Total Knee Arthroplasty

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07375472
Enrollment
140
Registered
2026-01-29
Start date
2025-01-14
Completion date
2026-01-10
Last updated
2026-01-30

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

Conditions

Postoperative Pain, Total Knee Arthroplasty

Keywords

virtual reality, distraction technique, postoperative pain, total knee arthroplasty, nursing intervention

Brief summary

This randomized controlled trial evaluates the effectiveness of three distraction techniques-virtual reality (VR) headset, squishy (squeeze toy), and poetry reading-on postoperative pain control in adults undergoing total knee arthroplasty. Participants are randomized into four parallel groups (three intervention arms and one usual care control). Pain intensity is assessed using the Visual Analog Scale (VAS), with primary assessment at 24 hours after surgery.

Detailed description

Total knee arthroplasty is a common orthopedic procedure that can be associated with significant postoperative pain. In addition to standard pharmacological analgesia, non-pharmacological approaches such as distraction techniques may help reduce perceived pain by redirecting attention away from nociceptive stimuli. This single-center, parallel-group randomized controlled trial will be conducted in the Orthopedics and Traumatology Clinic of Osmaniye State Hospital in Türkiye. Eligible adults (≥18 years) undergoing total knee arthroplasty will be randomized using a stratified block randomization approach based on baseline pain severity (VAS 0-3, 4-6, 7-10) to ensure balanced allocation across groups. The intervention arms include (1) VR headset distraction, (2) use of a squishy (squeeze toy) as a tactile distraction method, and (3) poetry reading as a cognitive distraction method. The control group receives usual postoperative care without a structured distraction intervention. All groups follow the same postoperative analgesia protocol. The primary outcome is postoperative pain intensity measured by VAS at 24 hours after surgery.

Interventions

BEHAVIORALVR Distraction

A supervised virtual reality distraction session delivered via a VR headset during postoperative hospitalization to support non-pharmacological pain management.

BEHAVIORALTactile Distraction With Squishy

Use of a squishy (squeeze toy) as a tactile distraction technique during postoperative hospitalization as part of non-pharmacological pain management.

BEHAVIORALPoetry Reading Distraction

Structured poetry reading conducted during postoperative hospitalization as a cognitive distraction approach to support non-pharmacological pain management.

Sponsors

Izmir Tinaztepe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Age 18 years or older * Undergoing total knee arthroplasty * Hospitalized in the postoperative period at Osmaniye State Hospital * Able to communicate and complete pain assessment (Visual Analog Scale) * Provides written informed consent * Managed under the same postoperative analgesia protocol and operated by the same surgeon (as per study protocol)

Exclusion criteria

* Severe cognitive impairment or inability to provide valid pain assessment * Postoperative complications that may interfere with participation or pain assessment * Contraindication to the assigned distraction method (e.g., intolerance to wearing a VR headset, severe nausea/dizziness, claustrophobia) * Refusal or withdrawal of consent

Design outcomes

Primary

MeasureTime frameDescription
Pain Intensity (VAS)24 hours after surgeryVisual Analog Scale pain score (0=no pain, 10=worst pain).

Secondary

MeasureTime frameDescription
Pain Intensity (VAS) by Pain Severity Strata24 hours after surgeryVAS pain score analyzed by baseline pain strata (0-3, 4-6, 7-10) using stratified allocation groups.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORSongül Gungor

Osmaniye State Hospital

STUDY_DIRECTORBerna Dizer

Izmir Tinaztepe University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026