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Artificial LimbsNCT03428815

Effects of Temperature Control Liner Materials on Long-Term Outcomes of Prothesis Use

A study testing Prosthesis suspension liner in people with Artificial Limbs and Skin Diseases, run by Goeran Fiedler at 1 site in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

This clinical trial will compare how many days per year people with lower limb prosthesis do not wear their prosthesis when fitted with a conventional liner and a liner made with phase change materials. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Artificial Limbs, Skin Diseases
What is being tested?
Prosthesis suspension liner
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
42 participants
Where
1 siteUnited States
Study dates
4 Feb 2019to 29 Sep 2020
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • use of a prosthesis with liner suspension,
  • at least one year of prosthesis use,
  • a well-fitting socket,
  • a matured residual limb (stable limb volume) that has not required socket modifications in the previous year,
  • the ability to walk with the prosthesis outdoors without notable limitations (K-Level 3),
  • stable weight,
  • absence of acute medical conditions that would temporarily affect the ability to use prostheses.

Who cannot join

  • use of a non-standard liner size,
  • current use of a PCM liner as the regular suspension system,
  • known allergies against liner materials,
  • any inability to understand the protocol and to comply with the associated tasks, such as maintaining a log of days when the prosthesis could not be used.
  • anticipated provision of a new prosthesis or extended (longer than one month) absences from the region during the study period

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Bakery Square MSPO labs

    Pittsburgh, Pennsylvania, 15206

Other trials in United States

About this study

This clinical trial will compare how many days per year people with lower limb prosthesis do not wear their prosthesis when fitted with a conventional liner and a liner made with phase change materials.

Read the detailed description

Background: The proposed work will generate evidence-based practice guidance for temperature control liner technologies and allow providers to optimize care to Service members and Veterans with limb loss. Sizeable numbers of Service members and Veterans live with limb loss, mostly due to traumatic musculoskeletal injury. Addressing the resulting functional deficit with prostheses increases the risk for secondary conditions such as pressure sores, impaired blood perfusion, and injuries from accidental falls. Any of those occurrences can render the prosthesis temporarily useless, making it challenging for users to engage in many activities of daily life, including work, exercise, and social participation. Many of the described issues originate at the interface between residual limb and prosthetic socket, where the objectives of sufficient weight distribution and suspension are conflicting with the necessity to facilitate heat exchange and limit contact pressure and friction.

Recently, prosthesis liners that contain phase-change material have become commercially available, holding the promise that the micro climate at the interface between the residual limb skin and the prosthetic socket can be regulated to reduce the users' tendency to sweat. Preliminary studies on these liners indicate that the socket temperatures inside the socket stayed lower and rose slower than in conventional liners. However, the clinical relevance of those findings remains unclear. While (perceived) socket comfort is certainly an important criterion in prosthesis fitting, it may be claimed that only tangible functional benefits are of concern.

Objective/Hypothesis: The purpose of this study is to investigate whether longer (6+ months) periods of use of phase-change material based temperature control liners have clinically meaningful effects.

It is hypothesized that use of phase-change material infused liners will improve prosthesis utilization (measured in days of prostheses use per time), physical performance (measured by 2-minute walk test), and self-reported prosthesis related quality of life (assessed by questionnaire). The research follows the rationale that lower and steadier skin temperatures should result in reduced sweat, friction, skin damage, and prosthesis abandonment. This would encourage users to wear their prosthesis for longer periods of time and for an expanded array of purposes, thus increasing their ability to ambulate and to engage in a greater variety of activities.

Specific Aims:

  1. To compare phase-change material liners to conventional liners with regard to activity and participation
  2. To quantify the effect of phase-change material liners on prosthesis related quality of life and physical performance over time
  3. To investigate the relationship between perceived benefits of phase-change material liners and patient-centric outcomes

Study Design: The proposed study will utilize a double-blind longitudinal cross-over research design. A sample of trans-tibial prosthesis users will be wearing their regular gel or silicone liners for six months and phase-change material liners for another six months in a randomized sequence. Their prostheses will be equipped with activity monitors, and participants will be asked to maintain a record of days when they could not wear their prosthesis due to any perceived issues with their residual limb or socket fit. In 1.5-month intervals, subjects' activity, physical performance, and overall prosthesis assessment will be recorded using standardized methods.

Being tested
Prosthesis suspension liner
Medical subject headings
Skin Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Prosthesis suspension linerDevice

    Liners out of phase change material will be fitted

Study groups in NCT03428815
Study groupRoleWhat they receive
PCM linerExperimentalWillowwood Smart Temp Liner
Receives: Device: Prosthesis suspension liner
regular linerActive comparatorUser's regular prescribed liner
Receives: Device: Prosthesis suspension liner

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Days Without Prosthesis

    Days with less than 10% of prosthesis steps than the individual's daily average across the study period. Days without prosthesis are prorated to a full year (365 days) for comparison purposes.

    Measured: 6 months

Secondary outcomes (1)
  1. Average Daily Step Count

    A participant's daily step counts were averaged across days with prosthesis use across each intervention period

    Measured: 6 months per intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Feb 2018
  2. Study start4 Feb 2019
  3. Primary completion30 Aug 2020
  4. Study completion29 Sep 2020

Why it stopped: Pandemic response invalidated long-term outcome data collection

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Crossover
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
42 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03428815
Sponsor's protocol ID
PRO17090574
Other IDs
W81XWH-16-OPORP-PORA
Status last verified
Feb 2021
First submitted
5 Feb 2018
Last updated
5 Mar 2021
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
Undecided: De-identified data may be shared in the future

Publications

  • Fiedler G, Singh A, Zhang X. Effect of temperature-control liner materials on long-term outcomes of lower limb prosthesis use: a randomized controlled trial protocol. Trials. 2020 Jan 10;21(1):61. doi: 10.1186/s13063-019-3920-4.

    PubMed 31924257

Questions about this trial

What is this clinical trial studying?

A study testing Prosthesis suspension liner in people with Artificial Limbs and Skin Diseases, run by Goeran Fiedler at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 5 Mar 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 5 Mar 2021). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Days Without Prosthesis (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03428815, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Mar 2021.

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