Effectiveness of an Exercise Program and Education Through a Mobile Application for the Management of Patients With Hand Osteoarthritis and Rheumatoid Arthritis

January 8, 2022 updated by: Alberto Marcos Heredia-Rizo, University of Seville

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

Strengthening and stretching exercise programs, and recommendations to protect the affected joint have shown to be effective both clinically and economically in conditions such as hand osteoarthritis and hand rheumatoid arthritis. However, their application format is not up to date. In this sense, problems such as the lack of monitoring by the health professional and the lack of patients motivation may cause poor adherence to the treatment protocol, which is one of the main predictors of treatment efficiency. Therefore, an smartphone application has been developed for the rehabilitation of hand osteoarthritis and rheumatoid arthritis to enhance patients adherence and motivation. The smartphone application includes: a) exercise programs and recommendations based on the most up to date scientific evidence adapted to the pathology; and b) enhancers of patient adherence to treatment (patient diaries and behavioral change strategies).The objective is to develop a cost effective digital solution to optimize the health care offered to these pathologies based on up to date scientific evidence in order to improve the functional ability and the quality of life of these patients, and to reduce the number of consultations to primary and specialized care.

Study Overview

Study Type

Interventional

Enrollment (Actual)

213

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Seville, Spain, 41009
        • Faculty of Medicine

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. 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;

      1. Hard tissue enlargement of 2 or more of 10 hand joints.
      2. Hard tissue enlargement of 2 or more interphalangeal joints.
      3. Fewer than 3 swollen Metacarpal joints.
      4. 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.
  2. 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:

      1. Morning stiffness in and around joints lasting at least 1 hour.
      2. Swelling in three or more joints.
      3. Swelling in hand or wrist joints,
      4. Symmetrical joint swelling.
      5. erosions or decalcification on radiographs of hand and/or wrist.
      6. Rheumatoid nodules.
      7. Abnormal serum rheumatoid factor.
    • Pain and dysfunction in the joints of the hands and/or wrists.
    • Possession of a smartphone with internet

Exclusion Criteria:

  1. 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)
  2. 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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
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.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
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
Change from Baseline Michigan Hand Questionnaire (MHQ) at 3 and 6 months
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
A self administered measure to assess hand pain, stiffness and functionality in persons with hand osteoarthritis
Change from Baseline Australian/Canadian (AUSCAN) Osteoarthritis Hand Index at 3 and 6 months

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
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
Change from Baseline Grip Strength at 3 months
Pinch strength assessed using a hydraulic pinch dynamometer
Time Frame: Change from Baseline Pinch strength at 3 months
The maximun power of the pinch muscles, pressing the tip thumb against the tip index finger, using an Hydraulic pinch dynamometer
Change from Baseline Pinch strength at 3 months
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
Amount of perceived pain represented on a scale of 0 (no pain) to 10 (worst pain)
Change from Baseline Visual Analog Scale of Pain at 1, 3 and 6 months
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
Amount of perceived stiffness represented on a scale of 0 (no stiffness) to 10 (worst stiffness)
Change from Baseline Visual Analog Scale of Stiffness at 3 and 6 months
Self-reported functional ability assessed by QuickDASH Questionnaire
Time Frame: Change from Baseline QuickDASH Questionnaire at 1, 3 and 6 months
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
Change from Baseline QuickDASH Questionnaire at 1, 3 and 6 months
Dexterity assessed using the Nine Hole Peg Test
Time Frame: Change from Baseline Nine Hole Peg Test at 3 months
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.
Change from Baseline Nine Hole Peg Test at 3 months
Quality of life assessed using the EQ-5D-5L questionnaire
Time Frame: Change from Baseline EQ-5D-5L Questionnaire at 3 and 6 months
A brief multi-attribute health status measure divided in five dimensions questions with Likert response options and a visual analog scale of Health
Change from Baseline EQ-5D-5L Questionnaire at 3 and 6 months
Economic factors relating to cost-utility
Time Frame: Change from Baseline Economic factors relating to cost-utility at 6 months
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
Change from Baseline Economic factors relating to cost-utility at 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2020

Primary Completion (Actual)

December 20, 2020

Study Completion (Actual)

February 25, 2021

Study Registration Dates

First Submitted

February 7, 2020

First Submitted That Met QC Criteria

February 7, 2020

First Posted (Actual)

February 11, 2020

Study Record Updates

Last Update Posted (Actual)

January 11, 2022

Last Update Submitted That Met QC Criteria

January 8, 2022

Last Verified

January 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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