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Functional Later Rehabilitation in Older Adults: Effectiveness of Physical Exercises (REATIVE)

Primary Purpose

Hip Fractures

Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Home-based physical exercise intervention
Control Group Usual Care
Sponsored by
Universidade Cidade de Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hip Fractures

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • After the first hip fragility fracture following a fall from standing height or while turning
  • Surgically treated in the later stage of rehabilitation phase (6 months up to 2 years after the fracture).

Exclusion Criteria:

  • Sustained a hip fracture trauma due to falls from higher surfaces or motor vehicle accidents or due to a tumors or disease (other than osteoporosis)
  • Several cognitive impairment, assessed by Mini-Mental State Examination adjusted for educational level [22];
  • Inability to walk, either with walking aid;
  • Progressive or severe neurological disease (e.g., Parkinson's disease, stroke);
  • Communication disability (several uncompensated visual or hearing deficits);
  • Medical condition contraindications exercise (e.g. unstable angina, severe valvular heart disease, large or expanding aortic aneurysm, etc.) [23];
  • Engaged in a regular exercise program, with a frequency more or equal than twice a week, 30 minutes a day (excluding walking and senior dance) [24].

Sites / Locations

  • Universidade Cidade de São PauloRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Home-based physical exercise

Control Group Usual Care

Arm Description

Participants randomized to the Intervention Group (IG) will be submitted to a physical exercise program involving a progressive and challenging balance training and a neuromuscular and functional training of the lower limbs, conducted at home by physiotherapists, once a week, lasting about one hour, in the first, second and third month after randomization and will be oriented to perform exercises, twice a week, through a booklet. Visits to follow up exercises progression will be conducted once a month, from de fourth to the sixth month and each two months until the end of the follow up at the 12th month, summing up 18 sessions. Participants will receive monthly phone calls to increase exercise adherence.

This group will receive usual care and the booklet regarding bone health information.

Outcomes

Primary Outcome Measures

Lower extremity function (Short Physical Performance Battery (SPPB)
will be measured by theSPPB [27], that consists of three blocks of tests that assess static balance, walking speed and, indirectly, the strength of the lower limbs (sitting and standing from a chair unassisted). Each test has a score of zero (worst performance) to 4 points (best performance), summing a total final score of 12 points. Change from baseline will be assessed at 6 and 12 months.

Secondary Outcome Measures

Physiological risk of falls (Profile Physiological Assessment long version (PPA)
will be measured by the PPA [12] which provides an overall score for risk of falling through a series of tests that evaluates the systems involved in the postural stability system. The results are computed on a software specifically developed for the test that generates a report assessing the risk of falls including 4 components: the individuals score on a global chart of fall risk, profile of the individuals performance in the tests, indicating in a table individuals performance in relation to the standards of the same age. Additionally, individual score for muscle strength, reaction time test, balance, sway and coordination will be also ascertained. Change from baseline will be assessed at 6 and 12 months.
Functional performance (WHO Disability Assessment Schedule (WHODAS II)
measured by the WHODAS II [29]. This scale measures the population health and functionality in 6 domains: cognition, mobility, self-care, interpersonal relationships, daily activities and participation. It was developed by WHO with theoretical model to the International Classification of Functioning, Disability and Health (ICF), and it is not intended for any specific health condition. This short version assesses the difficulty degree of performing 12 activities in past 30 days, which can be classified as none, mild, moderate, severe and extreme (cannot be performed). The degree of difficulty reported is based on the presence of increased effort, discomfort or pain, slowness or the presence of some change in the way of doing the activity. Change from baseline will be assessed at 6 and 12 months.
Quality of life (WHOQOL-bref)
measured by WHOQOL-bref [30], consists of 26 questions divided in 4 domains: physical, psychological, social relationships and environment. The questionnaire is based on the last 2 weeks of the participant and evaluated, for example, how safe he/she feel in her/his daily life and how satisfied is he/she with his/her ability to perform daily life activities. Change from baseline will be assessed at 6 and 12 months.
Physical activity intensity (Planned Exercise Questionnaire - IPEQ_W)
will be measured by the IPEQ_W [31], ten questions designed to measure physical activity planned and unplanned for older people. The version estimates the intensity of physical activity during the last week will be used. The participant will be questioned for the frequency (every day, 3-6 times per week, twice a week, once a week or less than once per week) and duration of activity (less than 15 minutes per day, more than 15 minutes and under 30 minutes per day, more than 30 minutes and less than 1 hour, less over 1 h and 2 h per day more and less than 4h per day 2h, 4h, and daily or more). The total score is derived by multiplying the frequency categories by categories of activity duration, expressed in hours per week. The ICC for the IPEQ_W total score was 0.81. The concurrent validity was adequate whereas the instrument was able to identify older people of different ages and degrees of disability. Change from baseline will be assessed at 6 and 12 months.
Occurrence of falls
will be assessed by monthly phone calls to participants. They will be encouraged to fill the diary that containing the record daily and the number of falls. A structured questionnaire will be used to identify possible falls and their consequences. The intervention group will be compared to control group at 6 and 12 months follow-up in relation to the number of falls, the incidence of falls and the proportion of elderly fallers. Change from baseline will be assessed at 6 and 12 months.
Usual gait speed (evaluate acceleration and deceleration using a stopwatch)
will be evaluated on a distance of 4.6 meters, including 2 meters for acceleration and 2 meters for deceleration using a stopwatch. The participant will be instructed to walk at their normal pace as if they were going to buy something at the grocery store. The time that the elderly takes to complete the course will be recorded three times. The computed velocity in meters per second will be calculated dividing the course in meters by the time taken to complete the course. The average of three attempts will be used. The use of walking aids will be allowed during the test [28]. Change from baseline will be assessed at 6 and 12 months.

Full Information

First Posted
November 3, 2014
Last Updated
November 25, 2017
Sponsor
Universidade Cidade de Sao Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT02295527
Brief Title
Functional Later Rehabilitation in Older Adults: Effectiveness of Physical Exercises
Acronym
REATIVE
Official Title
Effectiveness of a Physical Exercise Intervention Program in Improving Functional Mobility in Older Adults After Hip Fracture in Later Stage Rehabilitation: a Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Unknown status
Study Start Date
November 2014 (undefined)
Primary Completion Date
November 2018 (Anticipated)
Study Completion Date
December 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Cidade de Sao Paulo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hip fractures resulting from falls increase substantially with advancing age and less than a half of the elderly that have sustained and survived after the surgery regain their former levels of mobility. There is increasing evidence that rehabilitation interventions involving exercises and extended beyond the sub acute phase or even in a later stage of care have a positive impact on various functional abilities. The purpose of this study is to determine if an exercise program training for people who have suffered a fall-related hip fracture will improve functional mobility when compared with usual care. Randomized controlled trial using blinded assessors and intention-to-treat analysis. We will recruit 82 older adults, 60 years or over who have suffered a hip fracture due to a fall and have or have not completed physiotherapy and/or rehabilitation. These participants will be in a later stage rehabilitation phase (6 months up to 2 years after the fracture). Participants randomized to the Intervention Group (IG) will be submitted to a physical exercise program involving a progressive and challenging balance training and a neuromuscular and functional training of the lower limbs, conducted at home by physiotherapists, once a week, lasting about one hour, in the first, second and third month after randomization and will be oriented to perform exercises, twice a week, through a booklet. Visits to follow up exercises progression will be conducted once a month, from de fourth to the sixth month and each two months until the end of the follow up at the 12th month, summing up 18 sessions. Participants will receive monthly phone calls to increase exercise adherence. The control group will receive usual care. The primary outcome will be mobility-related disability and participants will be assessed in the baseline, at the end of the intervention (3 months), at 6 and 12 months. The participants will receive monthly phone calls to investigate falls and exercise adherence. Adverse effects will be monitored.
Detailed Description
Over a lifetime, about half of women and a quarter of men will suffer a fragility bone fracture [1, 2], mostly due to falling [2]. Among the most serious and common fractures are hip fractures, reaching significant levels of mortality [2] and disability [3]. Hip fracture is an increasingly important problem internationally, particularly in developing countries, due to the growth in the numbers of older people. It is estimated that in 2050 the global number of hip fractures will be between 7.3 and 21.3 million [4] and the cost with the treatment will be approximately of 131.5 billion dollars [5], due the population increase. Physical and psychological limitations post-fracture, such as decreased mobility [6] and muscle strength of lower limbs [7], deficit balance [6], lack of trust [7], fear of falling [6] and increased risk of falls [8], hamper around 40% of older people from returning to their daily activities to live independently and safely [3, 9]. Even after two years of injury, more than half of the elderly do not regain the functional level prior to injury [10], persisting with moderate to high risk of falls [6]. Risk of falls and future falls in this population may be due either to physical limitations [11, 12] (due to insufficient recovery of balance, muscle strength and consequently mobility) and the fact they have already suffered a fracture previously [13], further increasing the chances of new fractures in this population [14]. There is no consensus about the best intervention for functionality of the elderly after hip fracture. However, recently different exercise programs have been suggested to improve the mobility of these patients [8]. Some studies have shown the effectiveness of rehabilitation programs in the period of up to 6 months after injury [15-18]. Although, few studies have explored the late period rehabilitation (over 6 months) [19, 20], when functional limitations can persist due to inadequate dose as well as the type of exercise performed. Population in Brazil is growing age in one of the fastest rates in the world and will be even greater in the coming decades. The number of seniors will double between 2002 and 2020, from 15 million to 32 million and reach 64 million by 2050 (about 30% of the total population in Brazil) [21]. Furthermore, the elderly aged 80 and over will increase exponentially over the next four decades, putting a growing and disproportionate demand on the health system and social support [21]. The purpose of this study is to determine if an exercise program training for people who have suffered a fall-related hip fracture will improve functional mobility when compared with usual care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hip Fractures

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
82 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Home-based physical exercise
Arm Type
Experimental
Arm Description
Participants randomized to the Intervention Group (IG) will be submitted to a physical exercise program involving a progressive and challenging balance training and a neuromuscular and functional training of the lower limbs, conducted at home by physiotherapists, once a week, lasting about one hour, in the first, second and third month after randomization and will be oriented to perform exercises, twice a week, through a booklet. Visits to follow up exercises progression will be conducted once a month, from de fourth to the sixth month and each two months until the end of the follow up at the 12th month, summing up 18 sessions. Participants will receive monthly phone calls to increase exercise adherence.
Arm Title
Control Group Usual Care
Arm Type
Other
Arm Description
This group will receive usual care and the booklet regarding bone health information.
Intervention Type
Other
Intervention Name(s)
Home-based physical exercise intervention
Other Intervention Name(s)
REATIVE
Intervention Description
Progressive strengthening of muscle groups ankle dorsi flexors, knee extensors and hip abductors and progressive balance training according to individual capacity:weight-bearing, limits of stability, change of position/direction, maintenance of static and dynamic stability, anticipatory adjustments using different bases of support and different sensory conditions. Dynamic exercises involving spin on its own axis, sitting and standing, up and down stairs, functional reach, steps in different directions and walk training. In the first session the physiotherapist will choose two exercises that best address the participant function goals and will add more exercises each week according to the level of participants' ability and motivation. Participants will receive a detailed booklet, containing photos and instructions of the12 exercises.Visits to follow up exercises will be conducted by the physiotherapists to progress the exercises.
Intervention Type
Other
Intervention Name(s)
Control Group Usual Care
Other Intervention Name(s)
Usual care
Intervention Description
This group will receive usual care and will not have any disadvantage in participating in the study. We understand that usual care is what participant receives based on the network of health care in which he/she is inserted. The participants will receive at baseline assessment a diary falls logbook and a guidance booklet containing information about prevention of falls, fractures and bone health that will be explained at the moment.
Primary Outcome Measure Information:
Title
Lower extremity function (Short Physical Performance Battery (SPPB)
Description
will be measured by theSPPB [27], that consists of three blocks of tests that assess static balance, walking speed and, indirectly, the strength of the lower limbs (sitting and standing from a chair unassisted). Each test has a score of zero (worst performance) to 4 points (best performance), summing a total final score of 12 points. Change from baseline will be assessed at 6 and 12 months.
Time Frame
Change from baseline will be assessed at 6 and 12 months
Secondary Outcome Measure Information:
Title
Physiological risk of falls (Profile Physiological Assessment long version (PPA)
Description
will be measured by the PPA [12] which provides an overall score for risk of falling through a series of tests that evaluates the systems involved in the postural stability system. The results are computed on a software specifically developed for the test that generates a report assessing the risk of falls including 4 components: the individuals score on a global chart of fall risk, profile of the individuals performance in the tests, indicating in a table individuals performance in relation to the standards of the same age. Additionally, individual score for muscle strength, reaction time test, balance, sway and coordination will be also ascertained. Change from baseline will be assessed at 6 and 12 months.
Time Frame
Change from baseline will be assessed at 6 and 12 months
Title
Functional performance (WHO Disability Assessment Schedule (WHODAS II)
Description
measured by the WHODAS II [29]. This scale measures the population health and functionality in 6 domains: cognition, mobility, self-care, interpersonal relationships, daily activities and participation. It was developed by WHO with theoretical model to the International Classification of Functioning, Disability and Health (ICF), and it is not intended for any specific health condition. This short version assesses the difficulty degree of performing 12 activities in past 30 days, which can be classified as none, mild, moderate, severe and extreme (cannot be performed). The degree of difficulty reported is based on the presence of increased effort, discomfort or pain, slowness or the presence of some change in the way of doing the activity. Change from baseline will be assessed at 6 and 12 months.
Time Frame
Change from baseline will be assessed at 6 and 12 months
Title
Quality of life (WHOQOL-bref)
Description
measured by WHOQOL-bref [30], consists of 26 questions divided in 4 domains: physical, psychological, social relationships and environment. The questionnaire is based on the last 2 weeks of the participant and evaluated, for example, how safe he/she feel in her/his daily life and how satisfied is he/she with his/her ability to perform daily life activities. Change from baseline will be assessed at 6 and 12 months.
Time Frame
Change from baseline will be assessed at 6 and 12 months
Title
Physical activity intensity (Planned Exercise Questionnaire - IPEQ_W)
Description
will be measured by the IPEQ_W [31], ten questions designed to measure physical activity planned and unplanned for older people. The version estimates the intensity of physical activity during the last week will be used. The participant will be questioned for the frequency (every day, 3-6 times per week, twice a week, once a week or less than once per week) and duration of activity (less than 15 minutes per day, more than 15 minutes and under 30 minutes per day, more than 30 minutes and less than 1 hour, less over 1 h and 2 h per day more and less than 4h per day 2h, 4h, and daily or more). The total score is derived by multiplying the frequency categories by categories of activity duration, expressed in hours per week. The ICC for the IPEQ_W total score was 0.81. The concurrent validity was adequate whereas the instrument was able to identify older people of different ages and degrees of disability. Change from baseline will be assessed at 6 and 12 months.
Time Frame
Change from baseline will be assessed at 6 and 12 months
Title
Occurrence of falls
Description
will be assessed by monthly phone calls to participants. They will be encouraged to fill the diary that containing the record daily and the number of falls. A structured questionnaire will be used to identify possible falls and their consequences. The intervention group will be compared to control group at 6 and 12 months follow-up in relation to the number of falls, the incidence of falls and the proportion of elderly fallers. Change from baseline will be assessed at 6 and 12 months.
Time Frame
Change from baseline will be assessed at 6 and 12 months
Title
Usual gait speed (evaluate acceleration and deceleration using a stopwatch)
Description
will be evaluated on a distance of 4.6 meters, including 2 meters for acceleration and 2 meters for deceleration using a stopwatch. The participant will be instructed to walk at their normal pace as if they were going to buy something at the grocery store. The time that the elderly takes to complete the course will be recorded three times. The computed velocity in meters per second will be calculated dividing the course in meters by the time taken to complete the course. The average of three attempts will be used. The use of walking aids will be allowed during the test [28]. Change from baseline will be assessed at 6 and 12 months.
Time Frame
Change from baseline will be assessed at 6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: After the first hip fragility fracture following a fall from standing height or while turning Surgically treated in the later stage of rehabilitation phase (6 months up to 2 years after the fracture). Exclusion Criteria: Sustained a hip fracture trauma due to falls from higher surfaces or motor vehicle accidents or due to a tumors or disease (other than osteoporosis) Several cognitive impairment, assessed by Mini-Mental State Examination adjusted for educational level [22]; Inability to walk, either with walking aid; Progressive or severe neurological disease (e.g., Parkinson's disease, stroke); Communication disability (several uncompensated visual or hearing deficits); Medical condition contraindications exercise (e.g. unstable angina, severe valvular heart disease, large or expanding aortic aneurysm, etc.) [23]; Engaged in a regular exercise program, with a frequency more or equal than twice a week, 30 minutes a day (excluding walking and senior dance) [24].
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Monica R Perracini, Phd
Phone
+551121781565
Email
monica.perracini@unicid.edu.br
First Name & Middle Initial & Last Name or Official Title & Degree
Camila A Lima, Ms
Phone
+5511992105950
Email
camilabrown@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Monica R Perracini, Phd
Organizational Affiliation
Universidade Cidade de São Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universidade Cidade de São Paulo
City
São Paulo
State/Province
SP
ZIP/Postal Code
08371-110
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Monica R Perracini, Phd
Phone
+551121781565
Email
monica.perracini@unicid.edu.br
First Name & Middle Initial & Last Name & Degree
Camila A Lima
Phone
+5511992105950
Email
camilabrown@hotmail.com

12. IPD Sharing Statement

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27894271
Citation
Lima CA, Sherrington C, Guaraldo A, Moraes SA, Varanda RD, Melo JA, Kojima KE, Perracini M. Effectiveness of a physical exercise intervention program in improving functional mobility in older adults after hip fracture in later stage rehabilitation: protocol of a randomized clinical trial (REATIVE Study). BMC Geriatr. 2016 Nov 29;16(1):198. doi: 10.1186/s12877-016-0370-7.
Results Reference
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Functional Later Rehabilitation in Older Adults: Effectiveness of Physical Exercises

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