Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
NCT07036341

Rehabilitation After a Hip Fracture: the Effects of Dietary Protein and Exercise on Bone and Muscle Health and Quality of Life

Led by Wageningen University · Updated on 2025-06-25

102

Participants Needed

2

Research Sites

99 weeks

Total Duration

On this page

Sponsors

W

Wageningen University

Lead Sponsor

R

Rijnstate Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Hip fractures often lead to functional limitations, loss of independence, weight loss and decreased well-being. Only half of the patients regain their functional level and 24% die within the following year. Financial consequences are significant due to costly surgery and long-term care. Hip fracture incidence is expected to increase sharply due to the ageing population, reducing accessibility to and quality of rehabilitation care. Therefore, optimizing treatment is essential. Previous protein and exercise studies showed improved muscle and bone health in healthy or frail community-dwelling older adults, but effects in older hip fracture patients are not known. Better rehabilitation may improve bone and muscle health, nutritional status, quality of life, lower costs and lower burden for healthcare. The overall objective is to investigate the effectiveness, costs and cost-effectiveness of a protein-enriched diet and resistance exercise for 3 months compared to usual care on bone and muscle health, and quality of life in older adults recovering from an acute hip fracture.

CONDITIONS

Official Title

Rehabilitation After a Hip Fracture: the Effects of Dietary Protein and Exercise on Bone and Muscle Health and Quality of Life

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 65 years or older
  • Acute hip fracture
  • Able to provide written informed consent
  • Mentally competent as assessed by the treating physician
  • Admitted to a participating rehabilitation centre
Not Eligible

You will not qualify if you...

  • Allergy, intolerance, or hypersensitivity to milk or lactose (self-reported)
  • Unwilling to stop dietary supplements except calcium and vitamin D
  • Pathological or periprosthetic fracture
  • Abnormal liver or kidney function (eGFR <30 ml/min/1.73 m2)
  • Diagnosed with conditions where high protein intake is harmful (e.g., renal failure, liver disease)
  • Diagnosed bone metabolic disorders such as primary hyperparathyroidism, Paget's disease, or myeloma
  • Using medications other than bisphosphonates that strongly affect bone, calcium, or muscle metabolism
  • Having disorders that prevent following study protocol without caregiver help
  • Currently participating in other scientific research
  • No permission to access medical history and related information from healthcare providers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Rijnstate Hospital

Arnhem, Netherlands, 6851AD

Actively Recruiting

2

Gelderse Vallei Hospital

Ede, Netherlands, 6716RP

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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