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Effect of Leg Strengthening Exercise After Hip Fracture

A

Arcadia University

Status and phase

Completed
Phase 2
Phase 1

Conditions

Hip Fractures

Treatments

Other: TENS
Other: progressive resistance exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT00997776
MANGIONE-LEG STRENGTH 2006
1R03HD041944-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this trial was to examine the effectiveness of a short-term leg strengthening exercise program compared to attention control on improving leg strength, walking speed and endurance, physical performance, and physical function one year after hip fracture.

Full description

Poor functional outcomes are reported for the majority of older adults who sustain a hip fracture. The ability of hip fracture patients to make sustained functional improvements above and beyond natural recovery is unknown. It has been shown that gym-based programs can help old adults regain function after hip fracture. It is unclear if these results could be translated into the home setting that lacks the gym-based equipment, or if improvement would be sustainable. This program compares high intensity strength training performed in the home twice weekly for 10 weeks to an attention placebo control in which participants receive sensory electrical stimulation to leg muscles.

Enrollment

26 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Successful fixation (partial or total hip replacement or open reduction internal fixation) of a hip fracture within the last 6 months
  • Were 65 years of age or older, were living at home prior to the fracture, had a physician referral and were discharged from physical therapy.

Exclusion criteria

  • Medical history of unstable angina or uncompensated congestive heart failure, ongoing chemotherapy or renal dialysis, history of stroke with residual hemiplegia, Parkinson disease, absent sensation in the lower extremities due to sensory neuropathy, life expectancy of less than 6 months, and Folstein mental status scores < 20.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

26 participants in 2 patient groups

Exercise
Experimental group
Description:
High intensity lower extremity exercise
Treatment:
Other: progressive resistance exercise
Attention control
Sham Comparator group
Description:
lower extremity TENS
Treatment:
Other: TENS

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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