Neurocognitive Rehabilitation After Hip Replacement

Hip Osteoarthritis Clinical Trial

Official title:

Effectiveness of Neurocognitive Rehabilitation in Pain Management and Functional Recovery After Hip Replacement: Randomized Controlled Trial

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02231567
• Other study ID #: 3298/2014
• Status: Terminated
• Phase: N/A
• Start date: September 2014
• Est. completion date: December 2015

Study information

• Verified date: January 2016
• Source: University of Roma La Sapienza
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the study is to evaluate the effectiveness of an approach based on neurocognitive rehabilitation exercises in the form of sensory-motor problems, whose solution involves the use of higher cognitive functions (attention, memory, language), not required in a traditional approach proprioceptive, in order to obtain a more complete and long-lasting recovery.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 54
• Est. completion date: December 2015
• Est. primary completion date: December 2014
• Accepts healthy volunteers: No
• Gender: All
• Age group: 50 Years to 80 Years

Eligibility

Inclusion Criteria:

• Presence of symptomatic unilateral primary hip osteoarthritis treated with surgical replacement with a posterior-lateral approach and the use of a non-cemented prosthesis (press-fit). All the implants are composed of a stem Symax (Stryker-Howmedica) and a ceramic head with coupling ceramic-ceramic and are implanted by the same surgeon.

Exclusion Criteria:

• Different diagnosis from hip osteoarthritis (eg. Fracture)

• Concomitant osteoarthrosis of the hip or knee with gait restrictions

• Lameness for more than six months

• Central nervous system or Peripheral nervous system disorders

• Systemic inflammatory disorders (eg. Rheumatoid Arthritis)

• Systemic infectious disorders

• Cognitive impairment

• Neoplastic disorders

• Surgical revisions

• Intraoperative complications

• Suspected hip replacement infection

• Hip replacement with endoprosthesis.

Related Conditions & MeSH terms

• Hip Osteoarthritis
• Osteoarthritis, Hip

Intervention

Other:
• Neurocognitive Rehabilitation
The patients will be treated in inpatient clinic with a neurocognitive rehabilitation approach. The frequency will be two times a day for six days a week for four consecutive weeks. Followed by outpatient treatment three times a week for four weeks. Each session lasts about one hour.
• Traditional Rehabilitation
The patients will be treated in inpatient clinic with a traditional rehabilitation approach. The frequency will be two times a day for six days a week for four consecutive weeks. Followed by outpatient treatment three times a week for four weeks. Each session lasts about one hour.

Locations

Country	Name	City	State
Italy	Umberto I Hospital	Rome

Sponsors (1)

Lead Sponsor	Collaborator
University of Roma La Sapienza

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change of WOMAC Questionnaire from baseline to 24 weeks	Questionnaire for the assessment of pain, stiffness and physical function. It measures physical function and symptoms of the lower limb and explores the impact of disability and pain on activities of daily living. The questionnaire is self-administered and it is based on a metric scale ranging from 0 (no difficulty) to 100 (extreme difficulty).	baseline, 1 week, 8 weeks, 16 weeks, 24 weeks
Secondary	Change of Barthel Index from baseline to 24 weeks	Index for the evaluation of patient's performance in activities of daily living. The index is divided into eleven sub-categories that assess activities of daily living (ability to feed themselves, to ensure personal hygiene and dressing) and the mobility of the individual (gait, postural changes and transfers, stairs). For each item is assigned a score variable from full to reduced or absent functionality. The questionnaire is administered by an examiner and is based on a metric scale ranging from 0 (total dependence) to 100 (minimum dependence).	baseline, 1 week, 8 weeks, 16 weeks, 24 weeks
Secondary	Change of Visual Analogue Scale (VAS) from baseline to 24 weeks	It is based on a ten point scale, where 0 means no pain and 10 means the greatest pain ever. It enables the patients to express their pain intensity as numerical value.	baseline, 1 week, 8 weeks, 16 weeks, 24 weeks
Secondary	Change of SF-36 Health Survey Questionnaire from baseline to 24 weeks	Assessment of health status using the SF-36 Health Survey Questionnaire. The questionnaire is divided into eight sub-categories that measure the physical activity, role limitations due to physical health and emotional problems, physical pain, the perception of general health, vitality, social activities, mental health and changes in health status and two indices that summarize the overall assessment of the subject with respect to his physical health (ISF) and mental (ISM). Indices are derived from 8 subcategories evaluated and allow to summarize the results. The questionnaire is self-administered and subcategories is that the indices are based on a metric scale ranging from 0 (worst health status) to 100 (best health status) 17, 18.	baseline, 1 week, 8 weeks, 16 weeks, 24 weeks
Secondary	Change of Psychological Well-Being Questionnaire (PWB) from baseline to 24 weeks	Questionnaire for the assessment of psychological well-being and positive functioning of the individual. It includes 84 items and measures the six dimensions /scales of well-being proposed in the model developed by the American psychologist Carol Ryff: self-acceptance, positive interpersonal relationships, autonomy, environmental control, personal growth and purpose in life. The questionnaire is self-administered and each item is evaluated by a metric scale ranging from 1 (disagree) to 6 (totally agree). The negatively worded items are counted in reverse order. The sum score for each scale is calculated by summing the degree of agreement of each item.	baseline, 1 week, 8 weeks, 16 weeks, 24 weeks
Secondary	Change of parameters of Gait Analysis from baseline to 24 weeks	It's used to define the pattern of gait. The Gait Analysis provides different types of information such as quantitative kinematics data (angles of flexion-extension, abduction-adduction and external rotation of the main joints), velocity data (moments and powers the major joints) and electromyographic data.	baseline, 1 week, 8 weeks, 16 weeks, 24 weeks