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.
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
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:
- To compare phase-change material liners to conventional liners with regard to activity and participation
- To quantify the effect of phase-change material liners on prosthesis related quality of life and physical performance over time
- 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.
- Conditions
- Artificial Limbs, Skin Diseases
- 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 group | Role | What they receive |
|---|---|---|
| PCM liner | Experimental | Willowwood Smart Temp Liner Receives: Device: Prosthesis suspension liner |
| regular liner | Active comparator | User'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.
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)
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.
- First posted12 Feb 2018
- Study start4 Feb 2019
- Primary completion30 Aug 2020
- Study completion29 Sep 2020
Why it stopped: Pandemic response invalidated long-term outcome data collection
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Artificial LimbsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Goeran Fiedler
- Sponsor type
- University, hospital or other
- Collaborators
- Widener University, United States Department of Defense
- Responsible party
- Sponsor-investigator, Goeran Fiedler, University of Pittsburgh
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
- Results posted
- Yes, on ClinicalTrials.gov
- 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
Study at a glance
From the registry record, last updated by the sponsor on 5 Mar 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Temperature Control Liner Materials on Long-Term Outcomes of Prothesis Use
- ClinicalTrials.gov ID
- NCT03428815
- Acronym / sponsor ID
- PRO17090574
- Conditions
- Artificial Limbs, Skin Diseases
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Pandemic response invalidated long-term outcome data collection
- Enrolment
- 42 participants (actual)
- Lead sponsor
- Goeran FiedlerUniversity, hospital or other
- Collaborators
- Widener University, United States Department of Defense
- Study start
- 4 Feb 2019 (actual)
- Primary completion
- 30 Aug 2020 (actual)
- Study completion
- 29 Sep 2020 (actual)
- First posted
- 12 Feb 2018 (actual)
- Results
- Posted 5 Mar 2021
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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:
- To compare phase-change material liners to conventional liners with regard to activity and participation
- To quantify the effect of phase-change material liners on prosthesis related quality of life and physical performance over time
- 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.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| PCM liner | Experimental | Device: Prosthesis suspension linerWillowwood Smart Temp Liner |
| regular liner | Active comparator | Device: Prosthesis suspension linerUser's regular prescribed liner |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- 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),
Key exclusion criteria (5 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Prosthesis suspension linerLiners out of phase change material will be fitted | Device | PCM liner, regular liner |
Primary outcome
Days Without Prosthesis
Time frame: 6 months
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.
1 secondary outcome
Average Daily Step Count
Time frame: 6 months per intervention
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Mar 2021.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 31924257Fiedler 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.
- Details on the PLUS-M mobility scale used for baseline assessmentLink provided by the sponsor.
- Individual participant dataSharing planned: Undecided. De-identified data may be shared in the future
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
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.