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Context Effects in Exercise Therapy for Knee and/or Hip Pain (CONEX)

Primary Purpose

Joint Pain, Knee Pain, Hip Pain

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Contextually enhanced physical surroundings of exercise
Neuromuscular exercise
Sponsored by
University of Southern Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Joint Pain focused on measuring Joint pain, Context effects, Placebo effect, Exercise treatment

Eligibility Criteria

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

Inclusion Criteria:

  • Age: 35 years or older
  • Self-report of knee and/or hip pain within the last 3 months.
  • Willing and able to attend exercise therapy at the University of Southern Denmark, Odense M twice weekly.

Exclusion Criteria:

  • Co-morbidities or contraindication prohibiting to participation in exercise therapy.
  • Unable to fill-out questionnaires, or to speak, read or understand Danish.
  • Already participating in exercise therapy*, having had surgery to the hip/knee within the last 3 months or on waiting list for joint surgery within the coming 6 months. (*defined as supervised exercise program by physiotherapist, systematic strength training etc. with duration of 6 weeks or more)

Sites / Locations

  • Research Unit of Musculoskeletal Function and Physiotherapy, Department of Sports Science and Clinical Biomechanics, University of Southern Denmark

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

No Intervention

Arm Label

Exercise in standard room

Exercise in a contexually enhanced room

Waiting list

Arm Description

Intervention: Exercise Patients exercise in standard physical surroundings. The room is marked by years of use. The room is placed in the basement, has artificial lighting, poor acoustics and bare concrete walls.

Intervention: Exercise + contextually enhanced physical surroundings Patients exercise in a contextually enhanced room. The room has both artificial lighting and daylight, view of a recreational park, better acoustics, decorations among other factors, which may cause or enhance the context effect.

Patients on waiting list are included, baseline tested and placed on a waiting-list for a 8 week period and tested at 8 weeks follow-up. The group is representative of the natural cause of disease.

Outcomes

Primary Outcome Measures

Patients' Global Perceived Effect
Patients indicate their perception of the global effect of the intervention on a 7 point likert scale ranging from "substantially worse" to "no change" to "substantially improved". The scale is balanced around the 'no change' response with 3 steps in each direction, respectively deterioration or improvement.

Secondary Outcome Measures

Change from baseline in KOOS (The Knee injury and Osteoarthritis Outcome Score) or HOOS (The Hip Dysfunction and Osteoarthritis Score), respectively
Change from baseline in The 36-item Short-Form Health Survey (SF-36)
Change from baseline in Arthritis Self-Efficacy Scale
A modified version of the Arthritis Self-Efficacy Scale consisting of 11 items scoring patient reported self-efficacy
Patient satisfaction with physical surroundings
Patients are asked to indicate their level of satisfaction with different elements of the physical surroundings.

Full Information

First Posted
January 20, 2014
Last Updated
March 26, 2015
Sponsor
University of Southern Denmark
Collaborators
The Swedish Research Council, The Danish Rheumatism Association (funding)
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1. Study Identification

Unique Protocol Identification Number
NCT02043613
Brief Title
Context Effects in Exercise Therapy for Knee and/or Hip Pain
Acronym
CONEX
Official Title
Effect of Physical Surroundings on Effects From Exercise as Treatment for Hip or Knee Pain: A Double-blind Randomized Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
January 2015 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern Denmark
Collaborators
The Swedish Research Council, The Danish Rheumatism Association (funding)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study is designed to investigate the effect of physical surroundings on the effect of exercise therapy for knee and hip pain.
Detailed Description
Context effect have been shown to be influential in health-care settings, such as hospitals. This study investigates if context effects can be caused by the physical surroundings of exercise. The study is designed as a double-blind randomized controlled clinical trial. Patients with knee and/or hip pain with a duration of a least 3 months are included in the trial and randomly assigned to 3 groups. Exercise in pre-existing, standard room Exercise in contextually enhanced room. Waiting list. The intervention consists markedly different between the two exercise rooms. The physical surroundings are described by factors such as acoustics, light source and intensity, decorations and air quality. The exercise program applied is based on a previously investigated neuromuscular exercise program, NEMEX. The same program is performed in both exercise rooms. Consequently, only the physical surroundings differ between intervention groups. Patients' "global perceived effect" is used as the primary outcome assessed at 8 weeks follow-up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Joint Pain, Knee Pain, Hip Pain, Osteoarthritis, Knee, Osteoarthritis, Hip
Keywords
Joint pain, Context effects, Placebo effect, Exercise treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
103 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise in standard room
Arm Type
Active Comparator
Arm Description
Intervention: Exercise Patients exercise in standard physical surroundings. The room is marked by years of use. The room is placed in the basement, has artificial lighting, poor acoustics and bare concrete walls.
Arm Title
Exercise in a contexually enhanced room
Arm Type
Experimental
Arm Description
Intervention: Exercise + contextually enhanced physical surroundings Patients exercise in a contextually enhanced room. The room has both artificial lighting and daylight, view of a recreational park, better acoustics, decorations among other factors, which may cause or enhance the context effect.
Arm Title
Waiting list
Arm Type
No Intervention
Arm Description
Patients on waiting list are included, baseline tested and placed on a waiting-list for a 8 week period and tested at 8 weeks follow-up. The group is representative of the natural cause of disease.
Intervention Type
Other
Intervention Name(s)
Contextually enhanced physical surroundings of exercise
Intervention Description
Different physical surroundings of exercise may affects the patients differently and consequently influence the effect of exercise. The exercise rooms are different from each other on parameters such as source of lighting, acoustics, materials and decorations. The differences with the physical surroundings of exercise is the primary intervention for this study.
Intervention Type
Other
Intervention Name(s)
Neuromuscular exercise
Intervention Description
The neuromuscular exercise program is the same across the two exercise groups. Consequently, this intervention is not the primary intervention of this study. The exercise program is based on the previously reported NEMEX program designed for patients with hip or knee osteoarthritis, originally published by Ageberg et al, 2010 in BMCMusculoskeletal Disorders.
Primary Outcome Measure Information:
Title
Patients' Global Perceived Effect
Description
Patients indicate their perception of the global effect of the intervention on a 7 point likert scale ranging from "substantially worse" to "no change" to "substantially improved". The scale is balanced around the 'no change' response with 3 steps in each direction, respectively deterioration or improvement.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Change from baseline in KOOS (The Knee injury and Osteoarthritis Outcome Score) or HOOS (The Hip Dysfunction and Osteoarthritis Score), respectively
Time Frame
Baseline, 4 weeks, 8 weeks
Title
Change from baseline in The 36-item Short-Form Health Survey (SF-36)
Time Frame
Baseline, 4 weeks, 8 weeks
Title
Change from baseline in Arthritis Self-Efficacy Scale
Description
A modified version of the Arthritis Self-Efficacy Scale consisting of 11 items scoring patient reported self-efficacy
Time Frame
baseline, 4 weeks, 8 weeks.
Title
Patient satisfaction with physical surroundings
Description
Patients are asked to indicate their level of satisfaction with different elements of the physical surroundings.
Time Frame
8 weeks
Other Pre-specified Outcome Measures:
Title
Change from baseline in functional test: Single limb mini squat
Time Frame
Baseline, 8 weeks
Title
Change from baseline in functional test: Maximal number of knee bendings pr. 30 sec.
Time Frame
baseline, 8 weeks
Title
Change from baseline in functional test: Number of chair stands per. 30 sec.
Time Frame
baseline, 8 weeks
Title
Change from baseline in functional test: Timed 40 m walking test
Time Frame
baseline, 8 weeks
Title
Change from baseline in functional test: One leg hop for distance
Time Frame
Baseline, 8 weeks,
Title
Change from baseline in muscle strength, MVC knee extension
Time Frame
baseline, 8 weeks
Title
change from baseline in muscle strength, MVC, hip abduction
Time Frame
baseline, 8 weeks
Title
Change from baseline in aerobic capacity measured by a submaximal bicycle test by Aastrand & Saltin
Time Frame
Baseline, 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 35 years or older Self-report of knee and/or hip pain within the last 3 months. Willing and able to attend exercise therapy at the University of Southern Denmark, Odense M twice weekly. Exclusion Criteria: Co-morbidities or contraindication prohibiting to participation in exercise therapy. Unable to fill-out questionnaires, or to speak, read or understand Danish. Already participating in exercise therapy*, having had surgery to the hip/knee within the last 3 months or on waiting list for joint surgery within the coming 6 months. (*defined as supervised exercise program by physiotherapist, systematic strength training etc. with duration of 6 weeks or more)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Louise F. Sandal, MSc
Organizational Affiliation
Research Unit of Musculoskeletal Function and Physiotherapy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Research Unit of Musculoskeletal Function and Physiotherapy, Department of Sports Science and Clinical Biomechanics, University of Southern Denmark
City
Odense
ZIP/Postal Code
5230
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
20565735
Citation
Ageberg E, Link A, Roos EM. Feasibility of neuromuscular training in patients with severe hip or knee OA: the individualized goal-based NEMEX-TJR training program. BMC Musculoskelet Disord. 2010 Jun 17;11:126. doi: 10.1186/1471-2474-11-126.
Results Reference
background
PubMed Identifier
28768617
Citation
Sandal LF, Thorlund JB, Moore AJ, Ulrich RS, Dieppe PA, Roos EM. Room for improvement: a randomised controlled trial with nested qualitative interviews on space, place and treatment delivery. Br J Sports Med. 2019 Mar;53(6):359-367. doi: 10.1136/bjsports-2016-097448. Epub 2017 Aug 2.
Results Reference
derived
PubMed Identifier
25818278
Citation
Sandal LF, Thorlund JB, Ulrich RS, Dieppe PA, Roos EM. Exploring the effect of space and place on response to exercise therapy for knee and hip pain--a protocol for a double-blind randomised controlled clinical trial: the CONEX trial. BMJ Open. 2015 Mar 27;5(3):e007701. doi: 10.1136/bmjopen-2015-007701.
Results Reference
derived

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Context Effects in Exercise Therapy for Knee and/or Hip Pain

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