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Resiliency in Total Joint Arthroplasty

Utah System of Higher Education (USHE) logo

Utah System of Higher Education (USHE)

Status

Completed

Conditions

Osteoarthritis

Treatments

Other: StreaMD

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The investigators primary objective is to determine how does participation in StreaMD affect patient reported outcomes after Total Hip Arthroplasty (THA) or Total Knee Arthroplasty (TKA)?

Full description

Osteoarthritis is a leading cause of disability in the US. By conservative estimates, about 54 million adults in the US have doctor-diagnosed arthritis. The number of people expected to have arthritis by the year 2040 is more than 78 million. Total joint arthroplasty is considered the treatment of choice for end-stage osteoarthritis. Currently, more than 1 million hip and knee replacements are performed each year in the US. By 2030, primary THR is projected to grow 171% and primary TKR is projected to grow by up to 189%, for a projected 635,000 and 1.28 million procedures, respectively. The incidence of pre-operative psychological distress in this group of patients is reported between 30% and 60% and preoperative psychological distress is associated with poorer pain and functional outcomes after surgery. Resilience, characterized by an ability to bounce back or recover from stress, is increasingly recognized as a psychometric property affecting many outcomes' domains including outcomes after TJA. Better resilience could improve patients overall satisfaction with the procedure.

Enrollment

18 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients aged 18 and older who are receiving a total hip or knee replacement.

Exclusion criteria

  • Patients enrolled in the MyMobility study
  • Patients who do not have cell phones with text messaging capability
  • Non-English speaking patients

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

18 participants in 2 patient groups

Control
No Intervention group
Description:
No other non-standard of care activities will be performed
Intervention
Experimental group
Description:
Will be signed up for the automated text messaging program (StreaMD)
Treatment:
Other: StreaMD

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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