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Effects of Insoles in Patients With Rheumatoid Arthritis: Randomized Controlled Trial.

Primary Purpose

Rheumatoid Arthritis

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Custom Insoles
Standardized insoles
Sponsored by
University of Malaga
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rheumatoid Arthritis focused on measuring Rheumatoid arthritis, Foot, Insoles, Quality of life, Physical Activity

Eligibility Criteria

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

Inclusion Criteria:

  • More than 18 years of age
  • Early RA
  • To meet the criteria of American College of Rheumatology
  • History of bilateral subtalar and/or ankle and/or talonavicular pain
  • Informed consent
  • Normal range of motions at the ankle, subtalar, and midtarsal joints.

Exclusion Criteria:

  • Concomitant musculoskeletal disease
  • Central or peripheral nervous system disease
  • Endocrine disorders, especially diabetes mellitus with a level of insufficient foot sensitivity
  • Patients with a history of orthopedic foot surgery
  • Those currently using foot orthoses.
  • Patients with foot trauma in the last 6 months previous to the study
  • Vascular diseases affecting the foot, active synovitis and edema.
  • Normal daily walking aids will be not permitted.

Sites / Locations

  • University of MalagaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Custom insoles

Standardized insoles

Arm Description

Custom insoles will make with CAD-CAM using a laser scanning and casting for its construction. Custom insoles will make with direct adaptation technique (TAD) being of pvc resin.

Standardized insoles will be done by Ethylene-vinyl acetate (EVA) material.

Outcomes

Primary Outcome Measures

Change from Baseline Active graph (bracelet) at 3 months
This outcome will be measured with an activity monitor, accelerometer

Secondary Outcome Measures

Change from Baseline quality of life at 3 months
This outcome will be measured with a self-reported questionnaire (SF-36)
Change from Baseline foot function 3 months
This outcome will be measured with a self-reported questionnaire (foot function index)
Change from Baseline pain intensity at 3 months
This outcome will be measured with a self-reported questionnaire (Manchester foot pain and disability index)
Change from Baseline physical activity at 3 months
This outcome will be measured with a self-reported questionnaire (foot and ankle ability measure)

Full Information

First Posted
May 26, 2017
Last Updated
January 16, 2023
Sponsor
University of Malaga
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1. Study Identification

Unique Protocol Identification Number
NCT03170947
Brief Title
Effects of Insoles in Patients With Rheumatoid Arthritis: Randomized Controlled Trial.
Official Title
Effects of Insoles in Patients With Rheumatoid Arthritis Through Measurement of Quality of Life and Physical Activity: Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 21, 2022 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Malaga

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Deformity and foot pain is nearly omnipresent (90%) in rheumatoid arthritis (RA), due to the interaction between inflammation and abnormal biomechanical. These cause instability in the hindfoot, which cause deformity of the forefoot, and they cause more pressure on the plantar forefoot and more pain during daily activities. Non-pharmacological interventions (insole, footwear) have an important role, reducing pain and disability, increasing the effectiveness and improving daily activities.
Detailed Description
Randomized double-blind clinical trial. Two samples of patients will be taken: the control group, which will consist of patients with rheumatoid arthritis and standardized insoles, and other group, which will consist of patients with rheumatoid arthritis and insoles made with direct adaptation technique (TAD) and patients with rheumatoid arthritis and insoles made with an scanner (CAD-CAM). The variables that the investigators will measure are: age, sex, study level, current occupation, rheumatoid arthritis evolution time, quality of life and physical function, pain and health level and general function of the foot. The investigators will use: an accelerometer, and questionnaires: Foot and Ankle Ability Measures (FAAM), Manchester foot pain and disability index (MFPDI), Medical outcomes study short form-36 (SF-36) y Foot Function Index (FFI). This study will analyze patients in the Universities of Malaga and Salford for 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rheumatoid Arthritis
Keywords
Rheumatoid arthritis, Foot, Insoles, Quality of life, Physical Activity

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Custom insoles
Arm Type
Experimental
Arm Description
Custom insoles will make with CAD-CAM using a laser scanning and casting for its construction. Custom insoles will make with direct adaptation technique (TAD) being of pvc resin.
Arm Title
Standardized insoles
Arm Type
Active Comparator
Arm Description
Standardized insoles will be done by Ethylene-vinyl acetate (EVA) material.
Intervention Type
Device
Intervention Name(s)
Custom Insoles
Intervention Description
Custom insoles will make with CAD-CAM using a laser scanning and casting for its construction. All this needs the assistance of a computer. From the digital image of a positive of the limb in foam the insole will be obtained. Custom insoles make with direct adaptation technique (TAD) being of pvc resin. Once the resins are cut and with a temperature of 90º, they will be adapted to the foot (which will be protected with a sock) of the patient with the help of a vacuum. To this technique subtalar joint will be in a neutral position and metatarsal joints will be aligned.
Intervention Type
Device
Intervention Name(s)
Standardized insoles
Intervention Description
Standardized insoles were done by EVA material with shore of 18 and 180 kg/cm3 and manufactured, with an extension of 3/4. It was in contact with heel and plantar arch.
Primary Outcome Measure Information:
Title
Change from Baseline Active graph (bracelet) at 3 months
Description
This outcome will be measured with an activity monitor, accelerometer
Time Frame
one week, one month and three months
Secondary Outcome Measure Information:
Title
Change from Baseline quality of life at 3 months
Description
This outcome will be measured with a self-reported questionnaire (SF-36)
Time Frame
one week, one month and three months
Title
Change from Baseline foot function 3 months
Description
This outcome will be measured with a self-reported questionnaire (foot function index)
Time Frame
one week, one month and three months
Title
Change from Baseline pain intensity at 3 months
Description
This outcome will be measured with a self-reported questionnaire (Manchester foot pain and disability index)
Time Frame
one week, one month and three months
Title
Change from Baseline physical activity at 3 months
Description
This outcome will be measured with a self-reported questionnaire (foot and ankle ability measure)
Time Frame
one week, one month and three months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: More than 18 years of age Early RA To meet the criteria of American College of Rheumatology History of bilateral subtalar and/or ankle and/or talonavicular pain Informed consent Normal range of motions at the ankle, subtalar, and midtarsal joints. Exclusion Criteria: Concomitant musculoskeletal disease Central or peripheral nervous system disease Endocrine disorders, especially diabetes mellitus with a level of insufficient foot sensitivity Patients with a history of orthopedic foot surgery Those currently using foot orthoses. Patients with foot trauma in the last 6 months previous to the study Vascular diseases affecting the foot, active synovitis and edema. Normal daily walking aids will be not permitted.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Laura Ramos Petersen, Podiatry
Phone
686583936
Ext
+34
Email
lauraramos.94@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Gabriel Gijon Nogueron, PhD
Phone
951952872
Ext
+34
Email
gagijon@uma.es
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gabriel Gijon Nogueron, PhD
Organizational Affiliation
University of Malaga
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Malaga
City
Malaga
ZIP/Postal Code
29071
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabriel Gijon Nogueron, PhD
Phone
0034626449254
Email
gagijon@uma.es

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33560583
Citation
Ramos-Petersen L, Nester CJ, Ortega-Avila AB, Skidmore S, Gijon-Nogueron G. A qualitative study exploring the experiences and perceptions of patients with rheumatoid arthritis before and after wearing foot orthoses for 6 months. Health Soc Care Community. 2021 May;29(3):829-836. doi: 10.1111/hsc.13316. Epub 2021 Feb 9.
Results Reference
derived
PubMed Identifier
32690521
Citation
Ramos-Petersen L, Nester CJ, Gijon-Nogueron G, Ortega-Avila AB. Foot orthoses for people with rheumatoid arthritis, involving quantitative and qualitative outcomes: protocol for a randomised controlled trial. BMJ Open. 2020 Jul 19;10(7):e036433. doi: 10.1136/bmjopen-2019-036433.
Results Reference
derived

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Effects of Insoles in Patients With Rheumatoid Arthritis: Randomized Controlled Trial.

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