Trial document
DRKS00009251
Trial Description
Title
Effectiveness and efficiency of a group-based hip and knee training in combination with a structured home-exercise program for patients with hip or knee osteoarthritis: A controlled study in the context of health service research.
Trial Acronym
HKT
URL of the Trial
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Brief Summary in Lay Language
Osteoarthritis is the most common reason for pain in the elderly, and the individual and economic burden of this disease is immense. The chronic character of osteoarthritis requires a long-term therapeutic treatment. In this regard life-style interventions such as physical exercises that can be carried out by the patient himself are recommended as first line treatment. There is evidence for the short-term benefit of exercise therapy in terms of pain reduction and physical functioning.
For this reason the Health Insurance company AOK Baden-württemberg offers a country-wide health care offer for insurance holders with hip and/or knee osteoarthritis. The hip and knee program includes 8 supervised group sessions (up to 15 participants) complemented by a 11-week home-based exercise regime (2/week). Exercises aim for mobilization, strengthening and postural control.
This training will now be evaluated in the context of a study. Insurance holders participating in the program will be compared to insurance holders who do not participate. The aim of this study is to investigate, whether the hip and knee training is effective in terms of pain reduction and improvement of physical functioning among other things. It further ask for the cost-utility of the program and its safety. Outcomes are quantified by way of questionnaires. Economic data are derived from the insurance data base.
Participants of the study will be assessed at baseline and after 3 month and will further be followed up 6, 12 and 24 month after baseline.
Brief Summary in Scientific Language
Background: Osteoarthritis is the most common reason for pain in the elderly, and the individual and economic burden of this disease is immense. The chronic character of osteoarthritis requires a long-term therapeutic treatment. In this regard life-style interventions such as physical exercises that can be carried out by the patient himself are recommended as first line treatment. There is evidence for the short-term benefit of exercise therapy in terms of pain reduction and physical functioning. Nonetheless knowledge on long-term effects, dose-response-relationships as well as it’s cost-utility and safety is limited and are therefore under the scope of this study.
Methods/Design: This is a controlled study in the context of health service research. The study population consists of n = 1400 subjects with hip or knee osteoarthritis. The intervention group will be recruited from participants of a country-wide health insurance offer for people with hip or knee osteoarthritis. Potential participants for the control group will be selected from the insurance data base according to pre-defined matching criteria and asked by letter for their participation. The progressive training intervention comprises 8 supervised group sessions, supplemented by home exercises (2/week over 11 weeks). Exercises include mobilization, strengthening and training of postural control. Primary outcomes are pain and function measured with the WOMAC Index immediately after the intervention period. Among other things, health related quality of life, self-efficacy, cost utility and safety will be evaluated as secondary outcomes. Participants will also be followed up 6, 12 and 24 month after baseline.
Discussion: Results of this trial will document the effects of clinical as well as economic outcomes in a regular health care setting on the basis of a large sample size. As such, results of this trial will have great validity for sounded recommendations with respect to group- and home-based exercises in hip or knee osteoarthritis.
Do you plan to share individual participant data with other researchers?
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Description IPD sharing plan:
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Organizational Data
- DRKS00009251
- 2015/09/10
- [---]*
- yes
- Approved
- 421/2015BO1, Ethik-Kommission an der Medizinischen Fakultät der Eberhard-Karls-Universität und am Universitätsklinikum Tübingen
Secondary IDs
- [---]*
Health Condition or Problem studied
- M16 - Coxarthrosis [arthrosis of hip]
- M17 - Gonarthrosis [arthrosis of knee]
Interventions/Observational Groups
- The hip and knee program includes 8 supervised group sessions (up to 15 participants) each 1-1.5 hours, complemented by a 11-week home-based exercise regime (2/week). Exercises aim for mobilization, strengthening and postural control.
- General Care
Characteristics
- Interventional
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- Non-randomized controlled trial
- Open (masking not used)
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- Control group receives no treatment
- Treatment
- Other
- N/A
- N/A
Primary Outcome
Collection points: t0, t3 (number after t indicate month post baseline).
- WOMAC Index 3.1 German (11-box NRS): subscale pain
- WOMAC Index 3.1 German (11-box NRS): subscale physical functioning
Secondary Outcome
Collection points: t0, t3, t6, t12, t24 (number after t indicate month post baseline).
Clinical data:
- WOMAC Index 3.1 German (11-box NRS): subscale pain (t6, t12, t24)
- WOMAC Index 3.1 German (11-box NRS): subscale physical functioning (t6, t12, t24)
- WOMAC Index 3.1 German (11-box NRS): subscale physical stiffness
- WOMAC Index 3.1 German (11-box NRS): overall score
- Health related quality of life: VR-12 incl. VR-6D utility index (4-week-time-slot)
- Self-efficacy: General Self-Efficacy Scale (GSE)
- Responder analysis: Omeract-OARSI Set of - Responder Criteria (composite score with minimum absolute and relative change levels for pain or pain & function)
- Physical activity status: Habitual physical and sports activity status
- Time to surgery Endpoint: “elective joint replacement”
- Patient satisfaction: Modified version of the ZUF-8 Questionnaire
Economic data:
Cost categories: (1) intervention costs, (2) unspecific and (3) specific health care costs, (4) costs for days of disability
- Cost-Benefit Analysis (CBA) (intervention costs related to cost benefit of specific and unspecific health care costs and costs for days of disability)
- Cost-Effectiveness Analysis (CEA) (overall costs related to health related effects via WOMAC-Index)
- Cost-Utility Analysis (CUA) (overall costs related to quality adjusted life years (QALY)
Adherence to exercise
- Training log: Summarized number of attended training sessions
Safety evaluation
- Adverse events and side-effects: Summarized number and details of adverse events and side-effects
Countries of Recruitment
- Germany
Locations of Recruitment
- other
Recruitment
- Actual
- 2015/09/22
- 1400
- Multicenter trial
- National
Inclusion Criteria
- Both, male and female
- 18 Years
- no maximum age
Additional Inclusion Criteria
Lifetime prevalence of hip and/or knee OA diagnosed by a medical practitioner
Insurant of the insurance company offering the exercise program
Physical and mental ability to participate in the interventional program
Exclusion Criteria
- Significant established osteoporosis requiring treatment, previous spontaneous or low impact fracture
- Co-morbidities leading to major impairments in everyday life and representing contra-indications for physical activities
- Artificial joint replacement at the knee and/or hip joint within the last 6 months
- Surgery at the lower extremity within the last 3 months
- Regular use of gait aids
- Self-reported acute illness on t0
- Insufficient German language ability for self-administered questionnaires (IG)
- Current employment in the health care insurance
Exclusion criteria for primary data analysis only:
- < 15 points on the WOMAC Index, subscale pain (0-100) and < 15 points on the WOMAC Index, subscale physical functioning
In case of a previous artificial joint replacement at the hip and/or knee joint:
- Acute joint inflammation
- Instable anchoring of the artificial joint
- Radiologic signs of implant loosening
- Pain at rest or with activity due to artificial joint replacement at the knee and/or hip joint
- Luxation as an adverse event of artificial hip replacement
Addresses
-
start of 1:1-Block address primary-sponsor
- AOK Baden-Württemberg
- Presselstr. 19
- 70191 Stuttgart
- Germany
end of 1:1-Block address primary-sponsorstart of 1:1-Block address contact primary-sponsor- 07251-707150
- [---]*
- gerhard.mueller at bw.aok.de
- [---]*
end of 1:1-Block address contact primary-sponsor -
start of 1:1-Block address other
- Medizinische Universitätsklinik Tübingen, Abteilung Sportmedizin
- Hoppe-Seyler-Str. 6
- 72076 Tübingen
- Germany
end of 1:1-Block address otherstart of 1:1-Block address contact other- [---]*
- [---]*
- [---]*
- http://www.medizin.uni-tuebingen.de/sportmedizin/
end of 1:1-Block address contact other -
start of 1:1-Block address scientific-contact
- Medizinische Universitätsklinik Tübingen, Abteilung Sportmedizin
- Ms. PD Dr. Inga Krauß
- Hoppe-Seyler-Str. 6
- 72076 Tübingen
- Germany
end of 1:1-Block address scientific-contactstart of 1:1-Block address contact scientific-contact- 0049-7071-2986486
- 0049-7071-295162
- inga.krauss at med.uni-tuebingen.de
- http://www.medizin.uni-tuebingen.de/sportmedizin/
end of 1:1-Block address contact scientific-contact -
start of 1:1-Block address public-contact
- AOK Baden-Württemberg
- Mr. Dr. Gerhard Müller
- Bahnhofstraße 12-14
- 76646 Bruchsal
- Germany
end of 1:1-Block address public-contactstart of 1:1-Block address contact public-contact- 07251 707-150
- 0721 3711-91178
- Gerhard.Mueller at bw.aok.de
- [---]*
end of 1:1-Block address contact public-contact
Sources of Monetary or Material Support
-
start of 1:1-Block address materialSupport
- AOK Baden-Württemberg
- Presselstr. 19
- 70191 Stuttgart
- Germany
end of 1:1-Block address materialSupportstart of 1:1-Block address contact materialSupport- 07251-707150
- [---]*
- gerhard.mueller at bw.aok.de
- [---]*
end of 1:1-Block address contact materialSupport
Status
- Recruiting complete, follow-up complete
- 2019/09/11