CClinicalTrials.gg
CompletedNCT02022566Updated Mar 3, 2022Results posted

Effect of Structured Info and Adapted Exercise in OA

An interventional study of A supported self management of osteoarthritis program in Osteoarthritis, sponsored by Lund University. Completed at 1 site in Sweden. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2022-03-03.

Sponsored by Lund University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 years 8 months after the study started (first participant enrolled Apr 2009, registered Dec 2013).
Phase
Not applicable
Study type
Interventional
Enrollment
317
Allocation
Non-randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Physical activity level is measured at baseline and after 3 and 12 months after structured information and individually adapted exercise for patients with osteoarthritis in hip or knee.

The hypothesis of this study is that a supported self management of osteoarthritis program will increase the level of physical activity in patients with osteoarthritis in hip or knee. The second hypothesis is that patients with osteoarthritis in knee will increase their level of physical activity more than patients with osteoarthritis in hip.

Read the detailed description

Osteoarthritis (OA) is one of our most common chronic joint disorders. The World Health Organization (WHO) has estimated that every second woman and every fourth man over the age of 60 suffer some form of OA. OA is most common in hands, knee, hip and back. OA is a rheumatic disorder which affects the whole joint and may start as early as in the age of 30. The main symptoms are pain, stiffness and decreased quality of life.

The primary goals of OA management are to reduce the symptoms. Patient education and exercises are recommended as basic treatment according to national as well as international guidelines.

It is known that the level of physical activity decreases with age and that woman are less physical active than men. A study of healthy women older than 56 years showed that the level of activity decreased by 10 minutes per year, for every five year increase in age. OA is more common in women and is an irreversible disease, which means that the proportion of older women with osteoarthritis is large.

In addition OA is the most common cause of inactivity among the elderly and many fear that activity will further damage the joints. Inactivity is a large risk factor for poor physical and psychological health as well as premature death. Level of physical activity in people with OA has mainly been evaluated by self-assessment questionnaires. People with hip OA are more active than people with knee OA and the correlation between the degree of radiographic changes and physical activity is weak. Only 30% with early OA of the knee in the age group 35-65 years meet the recommendations for physical activity performed at least 30 minutes per day of moderate intensity, five days per week, measured by an accelerometer.

The primary aim of this study is to determine the effects of structured information and individually adapted exercises, delivered as a supported self-management osteoarthritis program, on overall levels of physical activity of moderate and vigorous intensity in patients with hip or knee OA. The secondary aim is to compare the level of physical activity in patients with hip and knee OA.

Supported self-management program for patients with osteoarthritis has been studied before and it's shown that it improves the quality of life, the physical function and decrease pain. No studies have investigated the effect of supported self-management on the level of physical activity.

This is an observational study with control group. Assessments are made at baseline and at 3 and 12 month after the supported self-management course.

The self-management program comprise three theoretical sessions, each of about 90 minutes, led by a physical therapist and held as group sessions with about 10 participants in each group. On the third session an osteoarthritis communicator participates. That is a person with osteoarthritis who communicate the lifestyle changes he/she have done to live a good life with OA. After the theoretical part the patients are offered an individually adapted exercise program, and the opportunity to practice this program together with others under supervision of a physical therapist twice per week for 6 weeks. Patients are also encouraged to find one or two exercises to perform continuously as home exercises. During the program home exercise and other alternatives as changing activity, using walking sticks, pain management ect are introduced in order to maintain the level of physical activity over an extended period of time. The importance of being physically active for a long time is accentuated in all aspects of the patient education. The primary aim of the supported self-management program is to increase the level of physical activity and empower patients to manage their disease, avoid illness and live a good life despite osteoarthritis.

Physical activity is measured with an accelerometer at baseline, 3 month and 12 month. We will also study the correlation between objectivity measured physical activity with physical activity questionnaire (UCLA), quality of life (EQ-5D), pain (VAS 0-100) and comorbidity.

All subjects in our study are also registered in a Swedish national quality register called Better management of patients with osteoarthritis (BOA). Some of the data used in the present study are collected from the register.

02

Conditions studied

  • Osteoarthritis

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Keywords

  • Osteoarthritis knee
  • Osteoarthritis hip
  • Physical activity
  • accelerometer
03

In context

Osteoarthritis

4,398 studies on the registry are indexed under Osteoarthritis; 582 are open to participants now.

This study's enrollment of 317 is above the median of 70 across 3,440 interventional studies indexed under Osteoarthritis.

Browse Osteoarthritis studies →

Lead sponsor

Lund University is the lead sponsor of 230 studies on the registry; 37 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Age between 18 and 75 years old.
  2. Patients with clinically verified OA, coming to see a physical therapist for the Supported self-management of osteoarthritis program.

Exclusion criteria

Exclusion Criteria:

  1. Other serious disorders causing hip or knee pain (e.g. tumor, rheumatic arthritis, sequel hip fracture).
  2. Other symptoms more aggravating than the OA problem (e.g. chronic pain, fibromyalgia, cardio-respiratory dysfunction, spinal condition).
  3. Total joint replacement surgery within the past 12 months.
  4. Other surgery of knee or hip within the past 3 months.
  5. Unable to read and understand Swedish and follow verbal and visual instructions.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
317 participants (actual)

Study arms

  • Experimental
    Supported self-management of osteoarthrits program

    Treatment with an supported self-management program for osteoarthritis.

    Behavioral: A supported self management of osteoarthritis program

  • No intervention
    Control group

    No intervention

Interventions

  • BehavioralA supported self management of osteoarthritis program

    Three theoretical sessions, each of about 90 minutes, held as group sessions with about 10 participants in each group. After the intervention patients are offered an individual exercise program, and the opportunity to practice this program together with others under supervision of a physical therapist for 6 weeks.

06

What researchers measure

Primary outcomes

  1. Level of Physical Activity/Sedentary Time

    The level of physical activity will be monitored by a GT1M Actigraph which is a small uniaxial accelerometer that measures vertical acceleration and deceleration. Accelerometer output is an activity "count" which is the weighted sum of the number of accelerations measured over a period (e.g. in this case 10 seconds). Participants will be instructed to wear the accelerometer from the morning, and continuously (except for water activities) until going to bed at night, for seven consecutive days. The accelerometer will be attached to a belt to wear around the waist with accelerometer placement on the right hip. The account of minutes in sedentary time will be calculated and the average of minutes in one week will be used.

    Time frame: Baseline, 3 months and 12 months

  2. Level of Physical Activity/Low Activity

    Level of physical activity will be monitored by an accelerometer at baseline and at 3 and 12 months after the supported self-management of osteoarthritis program using an accelerometer. The GT1M Actigraph is a small uniaxial accelerometer that measures vertical acceleration and deceleration. Accelerometer output is an activity "count" which is the weighted sum of the number of accelerations measured over a period (e.g. in this case 10 seconds). Participants will be instructed to wear the accelerometer from morning, and continuously (except for water activities) until going to bed at night, for seven consecutive days. The accelerometer will be attached to a belt to wear around the waist with accelerometer placement on the right hip.

    Time frame: baseline, 3 months and12 months

  3. Level of Physical Activity/Moderate-vigorous Activity

    Level of physical activity will be monitored by an accelerometer at baseline and at 3 and 12 months after the supported self-management of osteoarthritis program using an accelerometer. The GT1M Actigraph is a small uniaxial accelerometer that measures vertical acceleration and deceleration. Accelerometer output is an activity "count" which is the weighted sum of the number of accelerations measured over a period (e.g. in this case 10 seconds). Participants will be instructed to wear the accelerometer from morning, and continuously (except for water activities) until going to bed at night, for seven consecutive days. The accelerometer will be attached to a belt to wear around the waist with accelerometer placement on the right hip.

    Time frame: baseline, 3 month and 12 month

Secondary outcomes

  1. Health Realted Quality of Life

    To evaluate the health-related quality of life the EQ-5D-3L has been used. In this study, we have used the index of EQ-5D-3L with a British tariff. This scale is between (i.e., minimal value -0.594 (worst health), maximal value 1.00 (best health).

    Time frame: baseline, 3 months and 12 months

  2. Visual Analog Scale for Pain

    Visual Analog Scale for Pain has been used to evaluate pain. This is a scale from 0-100 mm there higher scores indicating higher intensity of pain. We have asked for the average pain the last month.

    Time frame: baseline, 3 months and 12 months

  3. Arthritis Self-efficacy Scale/Pain (ASES)

    The Arthritis Self-Efficacy Scale (ASES) is a widely used self-report measure of beliefs reflecting confidence in one's capacity to function despite pain and control pain or other symptoms of arthritis. ASES is scored on a 10-point Likert scale ranging from 10 (very uncertain=worst) to 100 (very certain=best).

    Time frame: baseline, 3 months and 12 months

07

Results

Posted Mar 3, 2022

Participant flow

Because of a large drop out from the Accelerometer assessment, we recruit more participants

Participant flow — Overall Study
MilestoneSupported Self-management of Osteoarthrits ProgramControl Group
Started22790
Completed16949
Not completed5841

Outcome measures

PrimaryLevel of Physical Activity/Sedentary Time

The level of physical activity will be monitored by a GT1M Actigraph which is a small uniaxial accelerometer that measures vertical acceleration and deceleration. Accelerometer output is an activity "count" which is the weighted sum of the number of accelerations measured over a period (e.g. in this case 10 seconds). Participants will be instructed to wear the accelerometer from the morning, and continuously (except for water activities) until going to bed at night, for seven consecutive days. The accelerometer will be attached to a belt to wear around the waist with accelerometer placement on the right hip. The account of minutes in sedentary time will be calculated and the average of minutes in one week will be used.

Time frame:
Baseline, 3 months and 12 months
Reported as:
Median · minutes
Level of Physical Activity/Sedentary Time
minutesSupported Self-management of Osteoarthrits ProgramControl Group
baseline562 (523 to 605)572 (505 to 599)
3 months556 (507 to 602)556 (504 to 592)
12 months552 (499 to 598)NA (NA to NA)
Statistical analysis
  • Supported Self-management of Osteoarthrits Program vs Control Group · ANOVA · p = <0.05
PrimaryLevel of Physical Activity/Low Activity

Level of physical activity will be monitored by an accelerometer at baseline and at 3 and 12 months after the supported self-management of osteoarthritis program using an accelerometer. The GT1M Actigraph is a small uniaxial accelerometer that measures vertical acceleration and deceleration. Accelerometer output is an activity "count" which is the weighted sum of the number of accelerations measured over a period (e.g. in this case 10 seconds). Participants will be instructed to wear the accelerometer from morning, and continuously (except for water activities) until going to bed at night, for seven consecutive days. The accelerometer will be attached to a belt to wear around the waist with accelerometer placement on the right hip.

Time frame:
baseline, 3 months and12 months
Reported as:
Median · minutes
Level of Physical Activity/Low Activity
minutesSupported Self-management of Osteoarthrits ProgramControl Group
baseline181 (150 to 214)169 (130 to 218)
3 months170 (144 to 205)169 (118 to 220)
12 months178 (140 to 228)NA (NA to NA)
Statistical analysis
  • Supported Self-management of Osteoarthrits Program vs Control Group · ANOVA · p = <0.05 · Mean difference (final values): 0.05
PrimaryLevel of Physical Activity/Moderate-vigorous Activity

Level of physical activity will be monitored by an accelerometer at baseline and at 3 and 12 months after the supported self-management of osteoarthritis program using an accelerometer. The GT1M Actigraph is a small uniaxial accelerometer that measures vertical acceleration and deceleration. Accelerometer output is an activity "count" which is the weighted sum of the number of accelerations measured over a period (e.g. in this case 10 seconds). Participants will be instructed to wear the accelerometer from morning, and continuously (except for water activities) until going to bed at night, for seven consecutive days. The accelerometer will be attached to a belt to wear around the waist with accelerometer placement on the right hip.

Time frame:
baseline, 3 month and 12 month
Reported as:
Median · minutes
Level of Physical Activity/Moderate-vigorous Activity
minutesSupported Self-management of Osteoarthrits ProgramControl Group
baseline34 (22 to 52)20 (11 to 30)
3 month34 (19 to 52)21 (10 to 37)
12 month32 (18 to 52)NA (NA to NA)
SecondaryHealth Realted Quality of Life

To evaluate the health-related quality of life the EQ-5D-3L has been used. In this study, we have used the index of EQ-5D-3L with a British tariff. This scale is between (i.e., minimal value -0.594 (worst health), maximal value 1.00 (best health).

Time frame:
baseline, 3 months and 12 months
Reported as:
Median · eq-5d index
Health Realted Quality of Life
eq-5d indexSupported Self-management of Osteoarthrits ProgramControl Group
baseline0.73 (0.62 to 0.80)0.66 (0.16 to 0.73)
3 months0.73 (0.69 to 0.80)0.52 (0.09 to 0.73)
12 months0.73 (0.69 to 0.80)NA (NA to NA)
SecondaryVisual Analog Scale for Pain

Visual Analog Scale for Pain has been used to evaluate pain. This is a scale from 0-100 mm there higher scores indicating higher intensity of pain. We have asked for the average pain the last month.

Time frame:
baseline, 3 months and 12 months
Reported as:
Median · units on a scale
Visual Analog Scale for Pain
units on a scaleSupported Self-management of Osteoarthrits ProgramControl Group
baseline51 (36 to 62)60 (50 to 70)
3 months37 (21 to 54)62 (37 to 71)
12 months38 (21 to 57)NA (NA to NA)
SecondaryArthritis Self-efficacy Scale/Pain (ASES)

The Arthritis Self-Efficacy Scale (ASES) is a widely used self-report measure of beliefs reflecting confidence in one's capacity to function despite pain and control pain or other symptoms of arthritis. ASES is scored on a 10-point Likert scale ranging from 10 (very uncertain=worst) to 100 (very certain=best).

Time frame:
baseline, 3 months and 12 months
Reported as:
Median · units on a scale
Arthritis Self-efficacy Scale/Pain (ASES)
units on a scaleSupported Self-management of Osteoarthrits ProgramControl Group
baseline60 (46 to 76)46 (38 to 62)
3 months74 (56 to 86)50 (32 to 70)
12 months68 (46 to 84)NA (NA to NA)
Post-hocArthritis Self-efficacy Scale/Other Symptoms

The Arthritis Self-Efficacy Scale (ASES) is a widely used self-report measure of beliefs reflecting confidence in one's capacity to function despite pain and control pain or other symptoms of arthritis. ASES is scored on a 10-point Likert scale ranging from 10 (very uncertain=worst) to 100 (very certain=best).

Time frame:
baseline, 3 months and 12 months
Reported as:
Median · units on a scale
Arthritis Self-efficacy Scale/Other Symptoms
units on a scaleSupported Self-management of Osteoarthrits ProgramControl Group
baseline68 (53 to 80)61 (48 to 70)
3 months76 (61 to 86)56 (46 to 81)
12 months71 (55 to 83)NA (NA to NA)

Adverse events

Collected over 12 month. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Supported Self-management of Osteoarthrits Program0/195 (0%)0/195 (0%)0/195 (0%)
Control Group0/69 (0%)0/69 (0%)0/69 (0%)

Baseline characteristics

The intervention group have been a part of a supported self-management of osteoarthritis and the control group were sign to meet a orthopedic doctor because of problems from knee or hip.

Age, Continuous
Age, Continuous(years)Supported Self-management of Osteoarthrits ProgramControl GroupTotal
Mean60 ± 1066 ± 764 ± 9
Sex/Gender, Customized
Sex/Gender, Customized(Participants)Supported Self-management of Osteoarthrits ProgramControl GroupTotal
female12540165
men702999
BMI
BMI(kg/m2)Supported Self-management of Osteoarthrits ProgramControl GroupTotal
Mean28 ± 528 ± 528 ± 5
Joint
Joint(Participants)Supported Self-management of Osteoarthrits ProgramControl GroupTotal
knee15238190
hip433174
Education
Education(Participants)Supported Self-management of Osteoarthrits ProgramControl GroupTotal
elementary school472471
high school7825103
university702090
Charnley Category (A=unilateral hip-OA, B=bilateral hip-OA, C=multiple joint OA
Charnley Category (A=unilateral hip-OA, B=bilateral hip-OA, C=multiple joint OA(Participants)Supported Self-management of Osteoarthrits ProgramControl GroupTotal
A552479
B8123104
C592281
Sedentary daily minutes
Sedentary daily minutes(minutes)Supported Self-management of Osteoarthrits ProgramControl GroupTotal
Median562 (523 to 605)572 (505 to 599)565 (520 to 602)
Low activity daily minutes
Low activity daily minutes(minutes)Supported Self-management of Osteoarthrits ProgramControl GroupTotal
Median180 (150 to 214)169 (130 to 218)178 (145 to 215)

5 further baseline measures are reported on the registry.

08

Study locations

1 site
  • Skånes universitets sjukhus
    Lund, 22241, Sweden
09

References and documents

Publications

  • Jonsson T, Ekvall Hansson E, Thorstensson CA, Eek F, Bergman P, Dahlberg LE. The effect of education and supervised exercise on physical activity, pain, quality of life and self-efficacy - an intervention study with a reference group. BMC Musculoskelet Disord. 2018 Jun 21;19(1):198. doi: 10.1186/s12891-018-2098-3. PubMed 30037339 ↗
10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 3, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT02022566
Lead sponsor
Lund University
Collaborators
Vastra Gotaland Region, The Swedish Rheumatism Ass
Responsible party
Sponsor
First posted
Dec 30, 2013
Start date
Apr 2009
Primary completion
Dec 2014
Completion
Jun 2018
Results posted
Mar 3, 2022
Last update
Mar 3, 2022

Study contacts

Carina A Thorstensson, Ass prof
principal investigator · Göteborg University
View the source record on ClinicalTrials.gov ↗

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