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Effect of the PainCoach App on Pain and Opiate Use After Total Knee Replacement

K

Kliniek ViaSana

Status

Completed

Conditions

E-health App
Opioid Use
Pain
Total Knee Replacement

Treatments

Behavioral: PainCoach app

Study type

Interventional

Funder types

Other

Identifiers

NCT03961152
PainCoach app study

Details and patient eligibility

About

Less is known about pain and opiate use at home directly after total knee replacement (TKR). Regarding side effects, low opiate use is desired. An e-health application, PainCoach app, was developed to guide patients in pain control and opiate use.

The aim of this study was to investigate the effect of the PainCoach app on pain and opiate use in TKR patients in the first two weeks at home after surgery. The hypothesis was that the use of this app would decrease pain and opiate use.

Enrollment

97 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Planned for primary TKR

Exclusion criteria

  • No possession of a smartphone or tablet
  • Contra-indication to any of the pain medication used in the study
  • No email address
  • No internet at home
  • No thorough command of the Dutch language
  • Suffering from memory disorders
  • Surgery under general anaesthesia

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

97 participants in 2 patient groups

PainCoach-app group
Experimental group
Description:
In the PainCoach-app group, in addition to receiving the aforementioned usual care, the PainCoach app was downloaded on each patient's smartphone or tablet. Patients could use this app whenever they wanted until day 14 after surgery. They were not subjected to any different treatment compared to the control group, i.e. advice on pain management was delivered in an extra and different way, but the pain medication itself was exactly the same for both groups.
Treatment:
Behavioral: PainCoach app
Control group
No Intervention group
Description:
The control group received usual care.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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