Prehabilitation in Older People Undergoing Total Hip Replacement

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age60+
SponsorUniversidad de La Frontera

About this trial

The goal of this clinical trial is to determine the effect of Resistance Exercise Training (RET)-based (p)rehabilitation versus usual care on skeletal muscle mass and function, as well as on underlying biological processes, in older adults undergoing elective Total Hip Replacement (THR) due to severe Osteoarthritis (OA). The main questions it aims to answer are:

* What is the effects of RET-based (p)rehabilitation versus usual care to improve muscle mass and function in patients undergoing elective unilateral THR surgery for end-stage OA? * What is the potential of certain circulating biomarkers to predict the efficacy of the musculoskeletal system response to RET in patients with severe OA? Researchers will compare RET-based (p)rehabilitation versus usual care to see if RET works to increase skeletal muscle mass and function.

Participants in the usual care group will undergo standard rehabilitation (12 weeks post-surgery), and participants in the (p)rehabilitation group will undergo RET-based full-body (p)rehabilitation (3x/week) for 2 weeks pre-surgery and 12 weeks post-surgery.

Eligibility criteria

Qualifiers

Individuals aged from 60 y and over.

18.5 < BMI < 40 kg/m2.

Individuals on waiting list to undergo a unilateral elective surgery for Total Hip Replacement due to primary severe Osteoarthritis.

Disqualifiers

Individuals with severe OA in the contralateral hip.

Individuals who has been performing regular RET (2 or more times per week) in the previous 6 months.

Individuals who smoke.

Significant psychiatric or neurological disorders, with the use of acetylcholinesterase inhibitors, and untreated mood disorders or depressive pathology.

Trial design

Treatments tested in this trial

  • (P)rehabilitation Progresive Resistance Exercise Training
  • Prehabilitation Group Deuterated Water
  • Usual Care Group Deuterated Water
  • Usual Care

Treatment groups

70 Participants
are divided into 2 treatment groups

Sponsors and collaborators