NCT07902206 · NOT YET RECRUITING

Creatine and Beta-Hydroxy-Beta-Methylbutyrate (HMB) Supplementation Plus Home-Based Exercise for Sarcopenia in Huntington's Disease

Sponsor: Universidad de Burgos

This trial tests whether creatine and HMB, two muscle-supporting supplements, taken alongside a 12-week home exercise program improve strength, physical function, and quality of life in people with Huntington's disease who have muscle loss or frailty. It has no phase label, meaning it is not a drug-approval study, and results will not be proven or final.

You may qualify if

  • Age 18 years or older with genetically confirmed Huntington's disease (HD) (cytosine-adenine-guanine [CAG] repeat expansion in the huntingtin [HTT] gene).
  • Symptomatic HD, defined by a Unified Huntington's Disease Rating Scale (UHDRS) total motor score > 4, in early-intermediate stages according to Total Functional Capacity (TFC).
  • Physical frailty and/or sarcopenia, defined as Short Physical Performance Battery (SPPB) score <= 10 and/or gait speed < 1.0 m/s and/or European Working Group on Sarcopenia in Older People 2 (EWGSOP2) sarcopenia criteria (low strength and low muscle quantity/quality assessed by validated bioelectrical impedance analysis (BIA)-derived indices).
  • VIVIFRAIL category B (frail) or C1/C2 (pre-frail).
  • Stable pharmacological treatment for at least 4 weeks before baseline.
  • Clinical judgement of the neurologist and occupational therapist that the participant can safely perform a prescribed home-based exercise program with weekly remote monitoring.
  • Written informed consent from the participant or legally authorized representative (with participant assent whenever possible).

You're excluded if

  • Unstable cardiovascular, renal, hepatic or musculoskeletal disease contraindicating exercise or supplementation.
  • Severe chorea or postural instability preventing safe training; uncontrolled psychiatric symptoms or active substance abuse.
  • Severe dysphagia preventing safe intake of thickened liquids (unless a clinically acceptable alternative exists).
  • Allergy or intolerance to any supplement component.
  • Pregnancy or lactation.
  • Use of protein supplements in the month before inclusion.

The sponsor's own eligibility wording, lightly reformatted. The study team makes the final eligibility decision — worth discussing with your doctor.

Eligibility criteria as of 2026-10-28

View full record on ClinicalTrials.gov

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