Skip to main content
OpenTrials
Active, Not Recruiting

NCT Number: NCT05196100

Acceptability of an Interim Socket System

This study will explore the acceptability of an interim socket system to new patients with a below-knee amputation and also to NHS healthcare providers.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Notify Me

Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospitals Dorset NHS Foundation Trust, Bournemouth, United Kingdom

Loading trial locations.

About this study

After a transtibial amputation, post-operative swelling, followed by muscle wasting, can lead to residual limb volume changes during the first 12 months. Managing this volume change often involves many socket modifications and/or replacement sockets. These multiple re-casts can be burdensome for the patient and delay recovery as patients are unable to mobilise and progress in an ill-fitting socket, leading to increased health resource use and costs.

An alternative technology exists involving an interim (aka confidence) socket whereby thermoplastic material is moulded onto the patient's residual limb and a socket is produced in a single session. This material can then be heated and remoulded quickly and comfortably, so that the patient accommodates to a single socket that can be adjusted as required to volume changes.

The confidence socket system could make the casting and prosthetic fitting process more efficient and cost-effective and improve the speed of delivery of the interim prosthesis. Thus a patient could start gait re-training with their confidence socket earlier compared to the standard treatment of fitting a laminate or polypropylene socket.

The aim of this pilot study is to assess the acceptability of the confidence socket to NHS healthcare providers and their patients, during an initial 3-month prosthetic fitting period.

Amputee participants will be recruited from 2 NHS sites. They will receive standard pre-prosthetic physiotherapy treatment until their primary MDT appointment, when they will be cast for their first prosthesis using the confidence socket which will replace standard care with the usual socket. Prescription of prosthetic foot components will continue as per usual care. Once the confidence socket is complete the patient will begin treatment according to usual physiotherapy rehabilitation. Amputee participants will be interviewed about their experience of receiving treatment with the confidence socket.

Healthcare providers delivering the treatment will also be interviewed about their acceptability of the confidence socket within the NHS pathways.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Over the age of 18
  • New transtibial amputation within the last 6 months
  • Deemed ready to cast for a prosthesis by the clinical team as per usual care at the prosthetic centre
  • Able to understand written English and provide informed consent

Exclusion criteria

  • Participants under the age of 18
  • Participants with an ankle disarticulation, Knee disarticulation or transfemoral amputation
  • Body mass > 125 kg with a distal circumference of 23-34 cm (small socket)
  • Body mass > 150 kg with a distal circumference of 30-45 cm (large socket)
  • Residual limb longer than 27 cm
  • Severe upper limb dysfunction (due to strength requirements to don the liner)
  • Severe visual requirements (that would restrict the person's ability to monitor their residual limb)
  • Contraindication to be fit for a prosthetic socket
  • Recent cerebrovascular event (i.e., stroke, haemorrhage, brain injury)
  • Disease affecting their memory
  • Unwilling to trial the confidence socket system
  • Unable to tolerate wearing a prosthetic liner due to excess sweating/ allergic reaction or other reasons

Treatment and study plan

Amparo confidence socket

Device

Confidence socket involves thermoplastic material being moulded onto the patient's residual limb and a socket is produced in a single session. The socket can be remoulded to adjust to changes in residual limb volume.

Primary outcomes

  1. Change in Socket comfort score

    Time frame: Up to 6 months

    Patient-reported socket comfort

Secondary outcomes

  1. Change in EQ-5D-5L

    Time frame: Up to 6 months

    Health related quality of life

  2. Change in Locomotor Capabilities Index (LCI-5)

    Time frame: Up to 6 months

    LCI-5 with prosthesis

  3. Change in Activities Balance Confidence-UK (ABC-UK)

    Time frame: Up to 6 months

    Balance confidence

  4. Change in L-test

    Time frame: Up to 6 months

    Functional timed up and go L-test

Sponsors and collaborators

Lead sponsor

University of Hull

Other

Collaborators

  • Portsmouth Hospitals NHS Trust
  • University Hospitals Dorset NHS Foundation Trust
  • University of Southampton

Registry information

Official study title

Acceptability of an Interim Socket System in the Immediate Rehabilitation of People With a tranSTibial Amputation (ASSIST): A Pilot Study

Acronym: ASSIST

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Jan 19, 2022
Registry last updated
Sep 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.