- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04263974
Effectiveness of an Exercise Program and Education Through a Mobile Application for the Management of Patients With Hand Osteoarthritis and Rheumatoid Arthritis
Effectiveness of a Mobile Application of Exercise and Education for the Management of Patients With Hand Osteoarthritis and Rheumatoid Arthritis on Self-reported Functional Ability, Dexterity, Pinch and Grip Strength, Pain Intensity and Stiffness
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Seville, Spain, 41009
- Faculty of medicine
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Hand Osteoarthritis (OA) patients:
Subjects with hand osteoarthritis according to the American College of Rheumatology (ACR) classification criteria for clinical OA; hand pain, aching or stiffness and 3 of the following points;
- Hard tissue enlargement of 2 or more of 10 hand joints.
- Hard tissue enlargement of 2 or more interphalangeal joints.
- Fewer than 3 swollen Metacarpal joints.
- Deformity of 1 or more of 10 hand joints.
- Pain and dysfunction in the joints of the hands and/or wrists
- Possession of a smartphone with internet.
Rheumatoid Arthritis (RA) Hand patients:
Subjects with hand arthritis according to the American College of Rheumatology (ACR) clinical and immunological criteria for clinical RA. Patients must meet 4 of the following seven criteria:
- Morning stiffness in and around joints lasting at least 1 hour.
- Swelling in three or more joints.
- Swelling in hand or wrist joints,
- Symmetrical joint swelling.
- erosions or decalcification on radiographs of hand and/or wrist.
- Rheumatoid nodules.
- Abnormal serum rheumatoid factor.
- Pain and dysfunction in the joints of the hands and/or wrists.
- Possession of a smartphone with internet
Exclusion Criteria:
Hand Osteoarthritis Patients:
- Age under 18 years
- People with cognitive impairment
- Surgery on any upper limb joint or fracture in the upper limb within the previous 6 months
- People on the waiting list for upper limb surgery.
- Persons who have received steroid injections into the joints of their hands in the two months prior to recruitment.
- People with inflammatory rheumatic disease (arthritis, spondylitis or cancer)
Rheumatoid Arthritis Hand Patients
- Age under 18 years
- People with cognitive impairment
- Surgery on any upper limb joint or fracture in the upper limb within the previous 6 months
- People on the waiting list for upper limb surgery.
- Pregnancy.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Smartphone Application
A protocol of exercises and general recommendations based on the current scientific evidence will be provided through a smartphone application. A follow-up of the use of the application will be carried out. The treatment protocol will last 6 months, during which a minimum of 4 weekly sessions of exercises will be carried out at home. Each pathology will have an unique program of exercises and recommendations. |
Exercises and recommendations, based on current scientific evidence, and delivered through the app for Smartphone called CareHand.
The intervention protocol is based on strengthening and stretching recommendations for rheumatoid arthritis and osteoarthritis in hands, transferred to an application format through explanatory videos together with tools to improve the autonomy, motivation and adherence of the patient
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Active Comparator: Conventional Treatment
Those in this group will received the conventional treatment protocol provided within the Andalusian Public Health System.
This will consist on the delivery of an exercise program and recommendations using a sheet of paper.
Participants will be told to perform the exercises during 6 months, with minimum of 4 weekly sessions of exercise that will be carried out at home.
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Conventional approach provided by the Andalusian Public Health System in Primary Care settings.
This approach consists of routine visits to the general practitioner specialist, and the delivery of an exercise sheet and recommendations.
This general mobility and stretching worksheet contains detailed images, as well as a description of how to perform the exercises and the dose to be taken.
While most exercises are intended for the wrist and hands, this sheet also includes basic exercises for the elbow joint.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Self reported functional ability assessed using Michigan Hand Questionnaire (MHQ) in patients with hand Rheumatoid Arthritis
Time Frame: Change from Baseline Michigan Hand Questionnaire (MHQ) at 3 and 6 months
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An outcome measurement tool specifically for chronic hand conditions providing information on functionality, satisfaction, appearance and perceived pain, with 37 questions divided into 6 subscales
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Change from Baseline Michigan Hand Questionnaire (MHQ) at 3 and 6 months
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Self reported functional ability assessed by Australian/Canadian (AUSCAN) Osteoarthritis Hand Index in patients with Hand Osteoarthritis
Time Frame: Change from Baseline Australian/Canadian (AUSCAN) Osteoarthritis Hand Index at 3 and 6 months
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A self administered measure to assess hand pain, stiffness and functionality in persons with hand osteoarthritis
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Change from Baseline Australian/Canadian (AUSCAN) Osteoarthritis Hand Index at 3 and 6 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Grip strength assessed using a hydraulic grip dynamometer
Time Frame: Change from Baseline Grip Strength at 3 months
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The Maximun power of the hand muscles used to firmly grasp an object by wrapping the fingers around it, pressing it against the palm, and using the thumb to apply counter-pressure, using a Hydraulic grip dynamometer
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Change from Baseline Grip Strength at 3 months
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Pinch strength assessed using a hydraulic pinch dynamometer
Time Frame: Change from Baseline Pinch strength at 3 months
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The maximun power of the pinch muscles, pressing the tip thumb against the tip index finger, using an Hydraulic pinch dynamometer
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Change from Baseline Pinch strength at 3 months
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Self reported pain assessed using a Visual Analog Scale of pain
Time Frame: Change from Baseline Visual Analog Scale of Pain at 1, 3 and 6 months
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Amount of perceived pain represented on a scale of 0 (no pain) to 10 (worst pain)
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Change from Baseline Visual Analog Scale of Pain at 1, 3 and 6 months
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Self reported stiffness assessed using a Visual Analog Scale of Stiffness
Time Frame: Change from Baseline Visual Analog Scale of Stiffness at 3 and 6 months
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Amount of perceived stiffness represented on a scale of 0 (no stiffness) to 10 (worst stiffness)
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Change from Baseline Visual Analog Scale of Stiffness at 3 and 6 months
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Self-reported functional ability assessed by QuickDASH Questionnaire
Time Frame: Change from Baseline QuickDASH Questionnaire at 1, 3 and 6 months
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Short form of the Disabilities of the Arm, Shoulder and Hand (DASH) Questionnaire.
A self administered outcome tool designed to measure physical function and symptoms in persons with musculoskeletal disorders of the upper limb
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Change from Baseline QuickDASH Questionnaire at 1, 3 and 6 months
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Dexterity assessed using the Nine Hole Peg Test
Time Frame: Change from Baseline Nine Hole Peg Test at 3 months
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Plastic instrument woth a shallow round dish to contain pegs and nine holes on the opposite side.
Consist of measuring the time spent to place and remove all the pegs from the holes.
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Change from Baseline Nine Hole Peg Test at 3 months
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Quality of life assessed using the EQ-5D-5L questionnaire
Time Frame: Change from Baseline EQ-5D-5L Questionnaire at 3 and 6 months
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A brief multi-attribute health status measure divided in five dimensions questions with Likert response options and a visual analog scale of Health
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Change from Baseline EQ-5D-5L Questionnaire at 3 and 6 months
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Economic factors relating to cost-utility
Time Frame: Change from Baseline Economic factors relating to cost-utility at 6 months
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Absence due to illness, absence from unpaid work, use of health resources (number of consultations to primary care, specialist doctor, physical therapy, occupational therapy, emergency department), pharmacological use for the pathology, medical or technical equipment purchased for the pathology
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Change from Baseline Economic factors relating to cost-utility at 6 months
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Collaborators and Investigators
Publications and helpful links
General Publications
- Rodriguez Sanchez-Laulhe P, Luque-Romero LG, Barrero-Garcia FJ, Biscarri-Carbonero A, Blanquero J, Suero-Pineda A, Heredia-Rizo AM. An Exercise and Educational and Self-management Program Delivered With a Smartphone App (CareHand) in Adults With Rheumatoid Arthritis of the Hands: Randomized Controlled Trial. JMIR Mhealth Uhealth. 2022 Apr 7;10(4):e35462. doi: 10.2196/35462.
- Rodriguez-Sanchez-Laulhe P, Luque-Romero LG, Blanquero J, Suero-Pineda A, Biscarri-Carbonero A, Barrero-Garcia FJ, Heredia-Rizo AM. A mobile app using therapeutic exercise and education for self-management in patients with hand rheumatoid arthritis: a randomized controlled trial protocol. Trials. 2020 Sep 10;21(1):777. doi: 10.1186/s13063-020-04713-4.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PI_RH_2018
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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