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CompletedNCT01088139Updated May 4, 2011

Nutritional Intervention for Geriatric Hip Fracture Patients

An interventional study of Protein supplementation in Hip Fractures, sponsored by Kowloon Hospital, Hong Kong. Completed at 1 site in Hong Kong. Open to participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2011-05-04.

Sponsored by Kowloon Hospital, Hong Kong · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
126
Allocation
Randomized
Ages
60 Years and older
Sex
All
01

Study summary

This is a randomized controlled, observer blinded trial to study the beneficial effect of nutritional supplementation in elderly Hong Kong patients after hip fracture surgery during rehabilitation and at 4 weeks follow up. The control group will receive Calcium and Vitamin D supplementation whereas the intervention group will receive a moderately high dose protein nutritional supplementation in addition to Vitamin D and Calcium. Both groups undergo the same rehabilitation program and dietary counseling before discharge. They are followed up 4 weeks after discharge or completion of supplementation. The outcome parameters are nutritional parameters and rehabilitation outcomes.

02

Conditions studied

  • Hip Fractures

Keywords

  • Nutritional support
  • Rehabilitation outcomes
03

In context

Fractures, Bone

2,261 studies on the registry are indexed under Fractures, Bone; 325 are open to participants now.

This study's enrollment of 126 is above the median of 69 across 1,482 interventional studies indexed under Fractures, Bone.

Browse Fractures, Bone studies →

Lead sponsor

Kowloon Hospital, Hong Kong is the lead sponsor of 9 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age 60 years or older
  • Recent low impact osteoporotic fracture of the proximal femur surgically repaired within 4 weeks before recruitment

Exclusion criteria

Exclusion Criteria:

  • Patients who require tube feeding
  • Patients in unstable medical condition
  • Body mass index (BMI) ≧ 25
  • Malignancy
  • Conditions with contraindication for high protein diet
  • Mentally incapacitated and inability to communicate or understand the consent.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
126 participants (actual)

Study arms

  • No intervention
    Control
  • Experimental
    Nutritional Supplementation

    Dietary Supplement: Protein supplementation

Interventions

  • Dietary supplementProtein supplementation

    Ready made protein supplement drinks with approximate protein content of 18-24g per 500ml per day. Caloric content is 490 to 530Kcal depending on the brand of drink.

    Also known as: Ensure (Abbott), Resource Breeze (Nestle Nutrition), Compleat (Nestle Nutrition), Glucerna (Abbott)

06

What researchers measure

Primary outcomes

  1. Nutritional parameters

    Biochemical and anthropometric measurements

    Time frame: Change from Baseline in nutritional parameters at discharge from hospital and at 4 weeks after discharge

Secondary outcomes

  1. Rehabilitation Outcomes

    functional, strength and mobility measurements

    Time frame: Change from Baseline in rehabilitation outcomes at discharge from hospital and at 4 weeks after discharge

07

Study locations

1 site
  • Department of Rehabilitation, Kowloon Hospital
    Kowloon, Hong Kong
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 4, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01088139
Lead sponsor
Kowloon Hospital, Hong Kong
First posted
Mar 17, 2010
Start date
Nov 2008
Primary completion
Mar 2010
Completion
Apr 2011
Last update
May 4, 2011

Study contacts

Ma Wai Wai MYINT, MBBS
principal investigator · Kowloon Hospital, Hong Kong

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2011. You cannot join it, but the record below documents what was studied.

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