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NCT03494127 | NOT YET RECRUITING | Mobility Impairment


User Evaluation of Advanced Personalized Modular Pressure Relief Seating Cushion Systems
Sponsor:

VA Office of Research and Development

Brief Summary:

30 Veterans who are full-time wheelchair users will use personalized modular cushions for two weeks each. Personalized cushions will be created using a cushion fitting process the investigators have already developed and tested. Microenvironmental conditions will be monitored during use. A cost analysis will ensure the customized modular cushion applies value-driven principles. User satisfaction will be measured along with the effects on daily function, skin status and seated tissue health.

Condition or disease

Mobility Impairment

Intervention/treatment

Use of GEL BALL FITTED MODULAR CUSHION

Use of SQUISHINS FITTED MODULAR CUSHION

Phase

NA

Detailed Description:

A repeated measures clinical study design will be carried out with 30 Veterans. 'Pre-baseline' seated interface pressures will be assessed with study participants sitting on their own cushions and pelvic region skin checks carried out by the study Research Nurse. All participants will then receive customized modular cushions. Participants will be randomly assigned to Group A or Group B using a modified randomization scheme. Group A participants will first use a gel ball fitted cushion for 2 weeks during all daily living activities while seated in their wheelchair followed by use of a SquishINS fitted cushion for 2 weeks. Group B will first use the SquishINS fitted cushion then a gel ball fitted cushion. Seated interface pressure distribution will be obtained at the beginning and end of each test period. A dual temperature and humidity sensor placed in the cushion will enable continuous monitoring of microenvironmental status during use. The study Research Nurse will repeat the pelvic region skin check and participants will complete a questionnaire based on the QUEST 2.0 user satisfaction instrument. All responses will be documented as part of the QS/DC program.

Study Type : INTERVENTIONAL
Estimated Enrollment : 30 participants
Masking : NONE
Primary Purpose : DEVICE_FEASIBILITY
Official Title : Development of Advanced Personalized Modular Pressure Relief Seating Cushion Systems: Testing and User Evaluation
Actual Study Start Date : 2025-08-23
Estimated Primary Completion Date : 2027-12-28
Estimated Study Completion Date : 2028-09-30

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Veterans with mobility impairments requiring full time use of a power or manual wheelchair who are served through the LSCDVAMC Wheeled Mobility Clinic.
Exclusion Criteria
  • * Pregnancy
  • * Inability to remain seated in the wheelchair for more than 4 hours/day

User Evaluation of Advanced Personalized Modular Pressure Relief Seating Cushion Systems

Location Details

NCT03494127


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Locations


Not yet recruiting

United States, Ohio

Louis Stokes VA Medical Center, Cleveland, OH

Cleveland, Ohio, United States, 44106-1702

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