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Effect of Cycle Ergometer in the Rehabilitation of Elderly Patients With Total Hip Arthroplasty

Effect of Cycle Ergometer in the Rehabilitation of Elderly Patients With Total Hip Arthroplasty: Randomized Controlled Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01622465
Enrollment
14
Registered
2012-06-19
Start date
2011-08-31
Completion date
2014-04-30
Last updated
2014-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis, Hip, Osteonecrosis

Keywords

Hip arthroplasty, Aged, Rehabilitation, Exercise therapy

Brief summary

The aim of this study is to evaluate the effects of an exercise program with a cycle ergometer in functional outcome and related-health quality of life (RHQL) in elderly patients with total hip arthroplasty.

Detailed description

Behavioral: Ergometer Cycling Ergometer Cycling under the guidance of a physical therapist after the second postoperative week. These training sessions were scheduled to be performed two times a week for a time period of at least eith weeks. Behavioral: No ergometer cycling Patients of the no ergometer cycling group did not receive any ergometer cycling after surgery, only conventional exercises.

Interventions

Patients will participate of the exercises program with ergometer cycling and conventional exercises. The program will initiate after two weeks of the postoperative and will continue until three months of the postoperative

BEHAVIORALConventional exercises

Patients will participate only of the conventional exercises program. The program will initiate after two weeks of the postoperative and will continue until three months of the postoperative

Sponsors

University of Campinas, Brazil
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged patients (60 years or more) of both sexes * Being submitted to the total hip arthroplasty, primary and unilateral, for hip osteoarthritis or hip osteonecrosis * no history of physical therapy two months before surgery

Exclusion criteria

* arthroplasty of hip fracture or other condition; * neurological disease that compromises motor function; * postoperative complications (dislocation, infection, cardiovascular events); * revision of the prosthesis; * patients who are unable to attend the sessions of physical therapy or refused to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in hip function at three monthsBaseline and three monthsHarris Hip Score (HHS) will be used to collect the data at baseline and at three months

Secondary

MeasureTime frameDescription
Change from baseline in physical performance of lower limbs at three months.Baseline and three monthsShort Physical Performance Battery (SPPB) developed by Guralnik (1994), to evaluate of balance, gait speed and muscle strenght, of lower limbs will be used to collect the data at baseline and at three months.
Change from baseline in health-related quality of life (HRQOL)at three months by generic questionnaireBaseline and three monthsThe generic questionnaire evaluation HRQOL Medical Outcomes Survey 36 - Item Short-Form developed by Ware and Sherboune (1992) will be used to collect the data at baseline and at three months
Change from baseline in health-related quality of life (HRQOL) at three months by specific questionnaireBaseline and three monthsThe specific questionnaire evaluattion HRQOL Western Ontario and McMaster Universities (WOMAC) developed by Bellamy (1988) will be used to collect the data at baseline and at three months.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026