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Resilience for Older Workers With OA Through Exercise

Resilience and Longevity for Older Workers With Arthritis Through Exercise

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02609672
Enrollment
24
Registered
2015-11-20
Start date
2015-08-31
Completion date
2016-07-31
Last updated
2018-03-22

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

Conditions

Osteoarthritis, Hip, Osteoarthritis, Knee

Keywords

Exercise, Resilience

Brief summary

Exercise is effective at reducing pain while improving physical function. However we do not know if exercise can boost resilience in the workplace, to allow people with osteoarthritis to work as long as they desire. Previous research shows that exercise holds the most promise for helping people enjoy their work because it reduces sick time, reduces pain, and improves productivity. However, little work has examined the effect of exercise for people with arthritis in the workplace. The purpose of the study is to investigate whether exercise improves resilience in the workplace, mobility, fitness, strength, and pain in comparison to no exercise in those with knee and/or hip osteoarthritis.

Detailed description

The Canadian workforce is aging. The most prevalent age group is 50-54 years and most of these Canadians will aim to continue working over the next 10 years. However, the impact of arthritis on aging Canadians compromises their ability to continue working. By 2031, over 2 million Canadians aged 45 to 64 years will have arthritis. We aim to boost the ability of older adults with the most common arthritis, osteoarthritis (OA), to engage in the workforce for as long as they desire. Identifying strategies to promote productivity among older workers with knee and hip OA will be of great public health significance in the coming decades. However, we face two challenges. First, obesity among sedentary workers is a risk for worsening knee and hip OA. Second, large occupational loads on the knee and hip worsen OA. Exercise has the most promise in addressing these challenges because it reduces pain and sick time, and improves mental health. Thus, there is a call for studies examining exercise for the aging worker with knee and hip OA. The purpose of this study is to examine the impact of an OA-specific leg strengthening exercise program, delivered within the workplace, on mobility, pain, physical capacity, and resilience among older workers with knee or hip OA.

Interventions

OTHERExercise

A biomechanical exercise program shown to decrease joint loading was administered 3 times a week for 12 weeks. Outcomes included mobility performance; pain; strength; cardiovascular fitness; and resilience.

OTHERNo Exercise

A no exercise (control) group maintained their existing activity level for 12 weeks. Outcomes included mobility performance; pain; strength; cardiovascular fitness; and resilience.

Sponsors

McMaster University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* 45 years of age or older * McMaster employee * Sedentary job (stand or walk for \<1/3 of work day) * Able to safely climb two flights of stairs * Hip pain * Hip pain during internal rotation and hip flexion * Knee pain * Less than 30 minutes of morning stiffness in the knee * Crepitus in the knee with active range of motion * Bony enlargement around the knee * Bony tenderness to palpation at the knee * No warmth around the knee

Exclusion criteria

* Any other forms of arthritis * Osteoporosis-related fracture * History of patellofemoral symptoms * Active non-arthritic hip or knee disease * Hip or knee surgery * Use of cane or walking aid * Unstable heart condition * Neurological conditions * Hip, knee or ankle injuries in past 3 months * Physician-advised restriction to physical activity * Any injuries that would prohibit participation in exercise * Ipsilateral ankle conditions * Currently receiving cancer treatment * Currently pregnant

Design outcomes

Primary

MeasureTime frameDescription
Change in Lower Extremity FunctionWeek 1 and Week 13The Lower Extremity Function Scale (LEFS) consists of 20 items, on an adjectival scale, that assess difficulty during mobility tasks ranging from transfers to running. Each item is scored from 0 (extreme difficulty or unable to perform activity), to 4 (no difficulty to perform activity). The minimum possible score is 0, and the maximum possible score is 80. Scores closer to 80 represent better self-reported physical function. It is reliable and valid in knee OA and has superior sensitivity to change compared to similar measures.

Secondary

MeasureTime frameDescription
Change in ResilienceWeek 1 and Week 13Resilience will be measured using the Resilience Scale 25 Survey, which is a 25-item questionnaire designed to evaluate a participants ability to adapt to stress and adversity. The test is scored out of 175 (scores ranging from 25 to 175), with higher scores indicating higher resilience.
Change in Mobility Performance (Six-Minute Walk Test)Week 1 and Week 13Mobility performance will be measured using the Six-Minute Walk Test (6MWT). For this test, participants are instructed to walk as far as possible in 6 minutes. The distance covered in 6 minutes is recorded in metres. This measure has produced reliable and valid data in persons with knee OA.
Change in Mobility Performance (40 Metre Walk Test)Week 1 and Week 13Mobility performance will be measured using the 40 Metre Walk Test. This test measures the time taken to complete a fast-paced 40 metre walk. The time taken to walk 40 metres is recorded in seconds. This measure has produced reliable and valid data in persons with knee OA.
Change in Mobility Performance (Stair Ascent)Week 1 and Week 13Mobility performance will be measured using the Stair Ascent Test. For this test, the time taken to ascend nine stairs is recorded in seconds. This measure has produced reliable and valid data in persons with knee OA.
Change in Mobility Performance (Stair Descent)Week 1 and Week 13Mobility performance will be measured using the Stair Descent Test. For this test, the time taken to descend nine stairs is recorded in seconds. This measure has produced reliable and valid data in persons with knee OA.
Change in Mobility Performance (30-second Chair Stand Test)Week 1 and Week 13Mobility performance will be measured using the 30-second Chair Stand Test. This test measures the number of times participants can rise and lower from a standard height chair, without using arm rests, in a 30-second period.This measure has produced reliable and valid data in persons with knee OA.
Change in Self-reported Knee and Hip PainWeek 1 and Week 13Change in self-reported knee and hip pain will be assessed with 3 valid and reliable questionnaires: the Knee injury and Osteoarthritis Outcome Score (KOOS), the Hip disability and Osteoarthritis Outcome Score (HOOS), and the Intermittent and Constant Osteoarthritis Pain (ICOAP) score. The KOOS and HOOS pain scores represent a normalized score from 0 (extreme symptoms) to 100 (no symptoms). KOOS and HOOS scores closer to 100 indicate fewer symptoms. The ICOAP consists of two sub-scales: constant pain (5 items) and intermittent pain (6 items). The score from each subscale represents a normalized score from 0 (no pain) to 100 (extreme pain). ICOAP scores closer to 0 indicate less pain. The items from each subscale are averaged to produce a normalized ICOAP total score, ranging from 0 (no pain) to 100 (extreme pain).
Change in Arthritis-related Self-efficacyWeek 1 and Week 13The Arthritis Self-Efficacy Scale (ASES) measures arthritis-specific beliefs regarding perception of performance on certain tasks to cope with the disease. The ASES is measured using 20 questions on a 10-100 scale with respect to three main areas: pain management (5 questions), physical function (9 questions), and other symptoms (6 questions). Each question is scored from 10 (very uncertain), to 100 (very certain), in 10-point increments. The minimum score for each subscale is 10, and the maximum score for each subscale is 100. The scores from each subscale are averaged to produce a normalized total score. Scores closer to 100 indicate greater certainty that a participant can cope with a particular task as a consequence of their disease.
Change in Depression StatusWeek 1 and Week 13Depression will be assessed with the Centre of Epidemiological Studies Depression (CES-D) Scale, a 20-item scale developed for the general population with emphasis on affect. Elements of affect include mood, guilt, worthlessness, helplessness, appetite, and sleep. Each item is scored from 0 (rarely or none of the time), to 3 (most of the time). The items are summed to produce a total score between 0 and 60 with a score of 16 or higher indicating depression.
Change in Grip Strength (Absolute)Week 1 and Week 13Grip strength will be assessed using a Jamar hand dynamometer. The hand dynamometer will be set to a fixed position and all values of grip force will be expressed in kg.
Change in Grip Strength (Relative)Week 1 and Week 13Grip strength will be assessed using a Jamar hand dynamometer. The hand dynamometer will be set to a fixed position and all values of grip force will be expressed in kg/kg (grip force/body mass).
Change in Isometric Knee and Hip Extensor and Flexor StrengthWeek 1 and Week 13The peak torque developed during knee and hip extension and flexion during a maximum isometric contraction will be measured by use of a Biodex System 2 isokinetic dynamometer. Data will be presented as Nm/kg (torque/body mass).
Change in Cardiovascular FitnessWeek 1 and Week 13Cardiovascular fitness will be calculated using the Single Stage Treadmill Walking Test. Predictions of VO2max will be made from heart rate (measured with a heart rate monitor), walking speed, age and gender.
Change in Mobility Performance (Timed Up and Go Test)Week 1 and Week 13Mobility performance will be measured using the Timed Up and Go Test. This test measures the time taken to rise from a standard chair with arm rests, walk 3 metres, and return to a seated position. This measure has produced reliable and valid data in persons with knee OA.

Countries

Canada

Participant flow

Participants by arm

ArmCount
Exercise
The participants in this arm were asked to attend 3 group classes per week for 12 weeks taught by a certified exercise instructor. Four class times were offered per week. These classes included a warm-up, static poses shown to decrease knee joint loading, and a cool down including flexibility exercises. Measurements were obtained at baseline (before intervention) and at follow-up (following intervention). Outcomes included clinical mobility; pain; isometric leg strength; cardiovascular fitness; and resilience. Exercise: A biomechanical exercise program shown to decrease joint loading was administered 3 times a week for 12 weeks. Outcomes included mobility performance; pain; strength; cardiovascular fitness; and resilience.
12
No Exercise
The participants in this arm were asked to refrain from changing their physical activity over the 12 weeks and maintain any strategies typically used to manage knee and/or hip pain. Since it is known that exercise is beneficial for pain management and strengthening in knee OA, participants randomized to the no exercise group were offered a free exercise pass following completion of the study. Measurements were obtained at baseline (before intervention) and at follow-up (following intervention). Outcomes included clinical mobility; pain; isometric leg strength; cardiovascular fitness; and resilience. No Exercise: A no exercise (control) group maintained their existing activity level for 12 weeks. Outcomes included mobility performance; pain; strength; cardiovascular fitness; and resilience.
12
Total24

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up31

Baseline characteristics

CharacteristicNo ExerciseExerciseTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
1 Participants0 Participants1 Participants
Age, Categorical
Between 18 and 65 years
11 Participants12 Participants23 Participants
Age, Continuous54.9 years
STANDARD_DEVIATION 6.7
52.8 years
STANDARD_DEVIATION 6.4
53.9 years
STANDARD_DEVIATION 6.5
Region of Enrollment
Canada
12 participants12 participants24 participants
Sex: Female, Male
Female
9 Participants10 Participants19 Participants
Sex: Female, Male
Male
3 Participants2 Participants5 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 120 / 12
serious
Total, serious adverse events
0 / 120 / 12

Outcome results

Primary

Change in Lower Extremity Function

The Lower Extremity Function Scale (LEFS) consists of 20 items, on an adjectival scale, that assess difficulty during mobility tasks ranging from transfers to running. Each item is scored from 0 (extreme difficulty or unable to perform activity), to 4 (no difficulty to perform activity). The minimum possible score is 0, and the maximum possible score is 80. Scores closer to 80 represent better self-reported physical function. It is reliable and valid in knee OA and has superior sensitivity to change compared to similar measures.

Time frame: Week 1 and Week 13

ArmMeasureValue (MEAN)Dispersion
ExerciseChange in Lower Extremity Function6.9 Change in scores on a scaleStandard Deviation 12.9
No ExerciseChange in Lower Extremity Function0.5 Change in scores on a scaleStandard Deviation 10.6
Secondary

Change in Arthritis-related Self-efficacy

The Arthritis Self-Efficacy Scale (ASES) measures arthritis-specific beliefs regarding perception of performance on certain tasks to cope with the disease. The ASES is measured using 20 questions on a 10-100 scale with respect to three main areas: pain management (5 questions), physical function (9 questions), and other symptoms (6 questions). Each question is scored from 10 (very uncertain), to 100 (very certain), in 10-point increments. The minimum score for each subscale is 10, and the maximum score for each subscale is 100. The scores from each subscale are averaged to produce a normalized total score. Scores closer to 100 indicate greater certainty that a participant can cope with a particular task as a consequence of their disease.

Time frame: Week 1 and Week 13

ArmMeasureGroupValue (MEAN)Dispersion
ExerciseChange in Arthritis-related Self-efficacyASES Pain1.1 Change in scores on a scaleStandard Deviation 2.5
ExerciseChange in Arthritis-related Self-efficacyASES Function0.9 Change in scores on a scaleStandard Deviation 1.4
ExerciseChange in Arthritis-related Self-efficacyASES Symptoms1.6 Change in scores on a scaleStandard Deviation 2.2
ExerciseChange in Arthritis-related Self-efficacyASES Total3.7 Change in scores on a scaleStandard Deviation 5.6
No ExerciseChange in Arthritis-related Self-efficacyASES Total1.6 Change in scores on a scaleStandard Deviation 3.2
No ExerciseChange in Arthritis-related Self-efficacyASES Pain0.6 Change in scores on a scaleStandard Deviation 2
No ExerciseChange in Arthritis-related Self-efficacyASES Symptoms0.9 Change in scores on a scaleStandard Deviation 1.5
No ExerciseChange in Arthritis-related Self-efficacyASES Function0.1 Change in scores on a scaleStandard Deviation 0.7
Secondary

Change in Cardiovascular Fitness

Cardiovascular fitness will be calculated using the Single Stage Treadmill Walking Test. Predictions of VO2max will be made from heart rate (measured with a heart rate monitor), walking speed, age and gender.

Time frame: Week 1 and Week 13

Population: Due to equipment problems, 2 participants from the Exercise Group were not able to complete the Single Stage Treadmill Walking Test.

ArmMeasureValue (MEAN)Dispersion
ExerciseChange in Cardiovascular Fitness-1.3 Change in ml/kg/minStandard Deviation 3
No ExerciseChange in Cardiovascular Fitness-1.7 Change in ml/kg/minStandard Deviation 2.5
Secondary

Change in Depression Status

Depression will be assessed with the Centre of Epidemiological Studies Depression (CES-D) Scale, a 20-item scale developed for the general population with emphasis on affect. Elements of affect include mood, guilt, worthlessness, helplessness, appetite, and sleep. Each item is scored from 0 (rarely or none of the time), to 3 (most of the time). The items are summed to produce a total score between 0 and 60 with a score of 16 or higher indicating depression.

Time frame: Week 1 and Week 13

ArmMeasureValue (MEAN)Dispersion
ExerciseChange in Depression Status-7.2 Change in scores on a scaleStandard Deviation 8
No ExerciseChange in Depression Status0.3 Change in scores on a scaleStandard Deviation 6.1
Secondary

Change in Grip Strength (Absolute)

Grip strength will be assessed using a Jamar hand dynamometer. The hand dynamometer will be set to a fixed position and all values of grip force will be expressed in kg.

Time frame: Week 1 and Week 13

ArmMeasureGroupValue (MEAN)Dispersion
ExerciseChange in Grip Strength (Absolute)Right Side Grip Strength1.1 Change in kgStandard Deviation 2.6
ExerciseChange in Grip Strength (Absolute)Left Side Grip Strength0.4 Change in kgStandard Deviation 3
No ExerciseChange in Grip Strength (Absolute)Right Side Grip Strength-0.1 Change in kgStandard Deviation 2.8
No ExerciseChange in Grip Strength (Absolute)Left Side Grip Strength-0.2 Change in kgStandard Deviation 2.8
Secondary

Change in Grip Strength (Relative)

Grip strength will be assessed using a Jamar hand dynamometer. The hand dynamometer will be set to a fixed position and all values of grip force will be expressed in kg/kg (grip force/body mass).

Time frame: Week 1 and Week 13

ArmMeasureGroupValue (MEAN)Dispersion
ExerciseChange in Grip Strength (Relative)Right Side Normalized Grip Strength0.0 Change in kg/kgStandard Deviation 0
ExerciseChange in Grip Strength (Relative)Left Side Normalized Grip Strength0.0 Change in kg/kgStandard Deviation 0
No ExerciseChange in Grip Strength (Relative)Right Side Normalized Grip Strength0.0 Change in kg/kgStandard Deviation 0
No ExerciseChange in Grip Strength (Relative)Left Side Normalized Grip Strength0.0 Change in kg/kgStandard Deviation 0
Secondary

Change in Isometric Knee and Hip Extensor and Flexor Strength

The peak torque developed during knee and hip extension and flexion during a maximum isometric contraction will be measured by use of a Biodex System 2 isokinetic dynamometer. Data will be presented as Nm/kg (torque/body mass).

Time frame: Week 1 and Week 13

ArmMeasureGroupValue (MEAN)Dispersion
ExerciseChange in Isometric Knee and Hip Extensor and Flexor StrengthKnee Extensor Torque (Nm/kg)0.1 Change in Nm/kgStandard Deviation 0.2
ExerciseChange in Isometric Knee and Hip Extensor and Flexor StrengthKnee Flexor Torque (Nm/kg)0.0 Change in Nm/kgStandard Deviation 0.1
ExerciseChange in Isometric Knee and Hip Extensor and Flexor StrengthHip Extensor Torque (Nm/kg)0.1 Change in Nm/kgStandard Deviation 0.2
ExerciseChange in Isometric Knee and Hip Extensor and Flexor StrengthHip Flexor Torque (Nm/kg)0.0 Change in Nm/kgStandard Deviation 0.1
No ExerciseChange in Isometric Knee and Hip Extensor and Flexor StrengthHip Flexor Torque (Nm/kg)0.0 Change in Nm/kgStandard Deviation 0.1
No ExerciseChange in Isometric Knee and Hip Extensor and Flexor StrengthKnee Extensor Torque (Nm/kg)-0.1 Change in Nm/kgStandard Deviation 0.2
No ExerciseChange in Isometric Knee and Hip Extensor and Flexor StrengthHip Extensor Torque (Nm/kg)0.1 Change in Nm/kgStandard Deviation 0.2
No ExerciseChange in Isometric Knee and Hip Extensor and Flexor StrengthKnee Flexor Torque (Nm/kg)0.0 Change in Nm/kgStandard Deviation 0.1
Secondary

Change in Mobility Performance (30-second Chair Stand Test)

Mobility performance will be measured using the 30-second Chair Stand Test. This test measures the number of times participants can rise and lower from a standard height chair, without using arm rests, in a 30-second period.This measure has produced reliable and valid data in persons with knee OA.

Time frame: Week 1 and Week 13

ArmMeasureValue (MEAN)Dispersion
ExerciseChange in Mobility Performance (30-second Chair Stand Test)0.2 Change in number of sit-to-stand cyclesStandard Deviation 2.4
No ExerciseChange in Mobility Performance (30-second Chair Stand Test)-0.5 Change in number of sit-to-stand cyclesStandard Deviation 2.5
Secondary

Change in Mobility Performance (40 Metre Walk Test)

Mobility performance will be measured using the 40 Metre Walk Test. This test measures the time taken to complete a fast-paced 40 metre walk. The time taken to walk 40 metres is recorded in seconds. This measure has produced reliable and valid data in persons with knee OA.

Time frame: Week 1 and Week 13

ArmMeasureValue (MEAN)Dispersion
ExerciseChange in Mobility Performance (40 Metre Walk Test)-0.7 Change in SecondsStandard Deviation 2.7
No ExerciseChange in Mobility Performance (40 Metre Walk Test)-0.1 Change in SecondsStandard Deviation 2.4
Secondary

Change in Mobility Performance (Six-Minute Walk Test)

Mobility performance will be measured using the Six-Minute Walk Test (6MWT). For this test, participants are instructed to walk as far as possible in 6 minutes. The distance covered in 6 minutes is recorded in metres. This measure has produced reliable and valid data in persons with knee OA.

Time frame: Week 1 and Week 13

ArmMeasureValue (MEAN)Dispersion
ExerciseChange in Mobility Performance (Six-Minute Walk Test)12.5 Change in MetresStandard Deviation 39.6
No ExerciseChange in Mobility Performance (Six-Minute Walk Test)23.7 Change in MetresStandard Deviation 54.1
Secondary

Change in Mobility Performance (Stair Ascent)

Mobility performance will be measured using the Stair Ascent Test. For this test, the time taken to ascend nine stairs is recorded in seconds. This measure has produced reliable and valid data in persons with knee OA.

Time frame: Week 1 and Week 13

ArmMeasureValue (MEAN)Dispersion
ExerciseChange in Mobility Performance (Stair Ascent)-0.4 Change in SecondsStandard Deviation 0.6
No ExerciseChange in Mobility Performance (Stair Ascent)0.0 Change in SecondsStandard Deviation 0.6
Secondary

Change in Mobility Performance (Stair Descent)

Mobility performance will be measured using the Stair Descent Test. For this test, the time taken to descend nine stairs is recorded in seconds. This measure has produced reliable and valid data in persons with knee OA.

Time frame: Week 1 and Week 13

ArmMeasureValue (MEAN)Dispersion
ExerciseChange in Mobility Performance (Stair Descent)-0.1 Change in SecondsStandard Deviation 0.4
No ExerciseChange in Mobility Performance (Stair Descent)0.0 Change in SecondsStandard Deviation 0.6
Secondary

Change in Mobility Performance (Timed Up and Go Test)

Mobility performance will be measured using the Timed Up and Go Test. This test measures the time taken to rise from a standard chair with arm rests, walk 3 metres, and return to a seated position. This measure has produced reliable and valid data in persons with knee OA.

Time frame: Week 1 and Week 13

ArmMeasureValue (MEAN)Dispersion
ExerciseChange in Mobility Performance (Timed Up and Go Test)-0.5 Change in SecondsStandard Deviation 1
No ExerciseChange in Mobility Performance (Timed Up and Go Test)0.2 Change in SecondsStandard Deviation 1
Secondary

Change in Resilience

Resilience will be measured using the Resilience Scale 25 Survey, which is a 25-item questionnaire designed to evaluate a participants ability to adapt to stress and adversity. The test is scored out of 175 (scores ranging from 25 to 175), with higher scores indicating higher resilience.

Time frame: Week 1 and Week 13

ArmMeasureValue (MEAN)Dispersion
ExerciseChange in Resilience6.2 Change in scores on a scaleStandard Deviation 16.5
No ExerciseChange in Resilience2.8 Change in scores on a scaleStandard Deviation 10.4
Secondary

Change in Self-reported Knee and Hip Pain

Change in self-reported knee and hip pain will be assessed with 3 valid and reliable questionnaires: the Knee injury and Osteoarthritis Outcome Score (KOOS), the Hip disability and Osteoarthritis Outcome Score (HOOS), and the Intermittent and Constant Osteoarthritis Pain (ICOAP) score. The KOOS and HOOS pain scores represent a normalized score from 0 (extreme symptoms) to 100 (no symptoms). KOOS and HOOS scores closer to 100 indicate fewer symptoms. The ICOAP consists of two sub-scales: constant pain (5 items) and intermittent pain (6 items). The score from each subscale represents a normalized score from 0 (no pain) to 100 (extreme pain). ICOAP scores closer to 0 indicate less pain. The items from each subscale are averaged to produce a normalized ICOAP total score, ranging from 0 (no pain) to 100 (extreme pain).

Time frame: Week 1 and Week 13

ArmMeasureGroupValue (MEAN)Dispersion
ExerciseChange in Self-reported Knee and Hip PainHOOS Pain4.1 Change in scores on a scaleStandard Deviation 7.3
ExerciseChange in Self-reported Knee and Hip PainICOAP Intermittent-26.4 Change in scores on a scaleStandard Deviation 17.2
ExerciseChange in Self-reported Knee and Hip PainICOAP Constant-20.6 Change in scores on a scaleStandard Deviation 23.1
ExerciseChange in Self-reported Knee and Hip PainICOAP Total Score-23.8 Change in scores on a scaleStandard Deviation 18.5
ExerciseChange in Self-reported Knee and Hip PainKOOS Pain8.3 Change in scores on a scaleStandard Deviation 13.3
No ExerciseChange in Self-reported Knee and Hip PainICOAP Total Score0.8 Change in scores on a scaleStandard Deviation 15
No ExerciseChange in Self-reported Knee and Hip PainKOOS Pain-1.0 Change in scores on a scaleStandard Deviation 6.4
No ExerciseChange in Self-reported Knee and Hip PainHOOS Pain0.2 Change in scores on a scaleStandard Deviation 13.3
No ExerciseChange in Self-reported Knee and Hip PainICOAP Constant-2.3 Change in scores on a scaleStandard Deviation 11.7
No ExerciseChange in Self-reported Knee and Hip PainICOAP Intermittent3.3 Change in scores on a scaleStandard Deviation 22

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026