A self-aligning prosthetic device for older patients with vascular-related amputations: Protocol for a randomised feasibility study (the STEPFORWARD study)

TY - JOUR

T1 - A self-aligning prosthetic device for older patients with vascular-related amputations: Protocol for a randomised feasibility study (the STEPFORWARD study)

AU - Mitchell, Natasha

AU - Coleman, Izzy

AU - Watson, Judith M

AU - Bell, Kerry Jane

AU - McDaid, Catriona Maria

AU - Barnett, Cleveland

AU - Twiste, Martin

AU - Jepson, Fergus

AU - Salawu, Abayomi

AU - Harrison, Dennis

AU - Vanicek, Natalie

N1 - © Author(s) (or their employer(s)) 2019.

PY - 2019/9/20

Y1 - 2019/9/20

N2 - Introduction The majority of older patients with a transtibial amputation are prescribed a standard (more rigid, not self-aligning) prosthesis. These are mostly suitable for level walking, and cannot adjust to different sloped surfaces. This makes walking more difficult and less energy efficient, possibly leading to longer term disuse. A Cochrane Review concluded there was insufficient evidence to recommend any individual type of prosthetic ankle-foot mechanism. This trial will establish the feasibility of conducting a large scale trial to assess the effectiveness and cost-effectiveness of a self-aligning prosthesis for older patients with vascular-related amputations and other health issues, compared to a standard prosthesis.Methods and analysisThis feasibility trial is a pragmatic, parallel group, randomised controlled trial (RCT) comparing standard treatment with a more rigid prosthesis versus a self-aligning prosthesis. The target sample size is 90 patients, who are aged 50 and over, and have a transtibial amputation, where amputation aetiology is mostly vascular-related or non-traumatic. Feasibility will be measured by: consent and retention rates, a plausible future sample size over a 24-month recruitment period, and completeness of outcome measures. Qualitative interviews will be carried out with trial participants to explore issues around study processes and acceptability of the intervention. Focus groups with staff at prosthetics centres will explore barriers to successful delivery of the trial. Findings from the qualitative work will be integrated with the feasibility trial outcomes in order to inform the design of a full-scale RCT.Ethics and dissemination Ethical approval was granted by Yorkshire & the Humber - Leeds West Research Ethics Committee on 4 May 2018. The findings will be disseminated via peer-reviewed research publications, articles in relevant newsletters, presentations at relevant conferences and the patient advisory group. Trial registration ISRCTN15043643 Keywords Randomised controlled trial, feasibility, amputation, prosthesis, acceptability, vascular Protocol versionVersion 1.3, 27th November 2018

AB - Introduction The majority of older patients with a transtibial amputation are prescribed a standard (more rigid, not self-aligning) prosthesis. These are mostly suitable for level walking, and cannot adjust to different sloped surfaces. This makes walking more difficult and less energy efficient, possibly leading to longer term disuse. A Cochrane Review concluded there was insufficient evidence to recommend any individual type of prosthetic ankle-foot mechanism. This trial will establish the feasibility of conducting a large scale trial to assess the effectiveness and cost-effectiveness of a self-aligning prosthesis for older patients with vascular-related amputations and other health issues, compared to a standard prosthesis.Methods and analysisThis feasibility trial is a pragmatic, parallel group, randomised controlled trial (RCT) comparing standard treatment with a more rigid prosthesis versus a self-aligning prosthesis. The target sample size is 90 patients, who are aged 50 and over, and have a transtibial amputation, where amputation aetiology is mostly vascular-related or non-traumatic. Feasibility will be measured by: consent and retention rates, a plausible future sample size over a 24-month recruitment period, and completeness of outcome measures. Qualitative interviews will be carried out with trial participants to explore issues around study processes and acceptability of the intervention. Focus groups with staff at prosthetics centres will explore barriers to successful delivery of the trial. Findings from the qualitative work will be integrated with the feasibility trial outcomes in order to inform the design of a full-scale RCT.Ethics and dissemination Ethical approval was granted by Yorkshire & the Humber - Leeds West Research Ethics Committee on 4 May 2018. The findings will be disseminated via peer-reviewed research publications, articles in relevant newsletters, presentations at relevant conferences and the patient advisory group. Trial registration ISRCTN15043643 Keywords Randomised controlled trial, feasibility, amputation, prosthesis, acceptability, vascular Protocol versionVersion 1.3, 27th November 2018

UR - https://bmjopen.bmj.com/content/bmjopen/9/9/e032924.full.pdf

U2 - 10.1136/bmjopen-2019-032924

DO - 10.1136/bmjopen-2019-032924

M3 - Article

SN - 2044-6055

JO - BMJ Open

JF - BMJ Open

ER -