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Implementation of the D-Foot at the Department of Prosthetics and Orthotics

S

Sahlgrenska University Hospital

Status

Completed

Conditions

Diabetic Foot

Treatments

Procedure: Conventional foot screening
Procedure: The D-Foot method

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Early identification of potential risk factors for the onset of diabetic foot ulcers are recommended. However, in a Swedish context, there has been no standardised routines to be used in the foot screening procedure. In this study a new standardised routine, the D-Foot, will be tested at the Department of Prosthetics and Orthotics. The usability of the web program will be tested.

Full description

The primary research questions are"how do patients with diabetes perceive the foot screening?" and "do the perception differ in the group that was foot screened by the use of the D-Foot compared to the group that was foot screened with conventional methods?"

Enrollment

111 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diabetes
  • patients referred to the Department of Prosthetics and Orthotics at Sahlgrenska University Hospital with the aim to be provided with assistive devices with the purpose to protect the feet from foot ulcers
  • be able to read and understand the Swedish language

Exclusion criteria

*being unable to read and understand the Swedish language

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

111 participants in 2 patient groups

The D-Foot method
Experimental group
Description:
The patients are being foot screened following the routine that is programmed in the D-Foot.
Treatment:
Procedure: The D-Foot method
Conventional foot screening
Active Comparator group
Description:
The patients are being foot screened according to conventional methods.
Treatment:
Procedure: Conventional foot screening

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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