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Knee Osteoarthritis and Balneotherapy (ANGELLO)

Primary Purpose

Knee Osteoarthritis

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Balneotherapy program
Sponsored by
CEN Biotech
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Knee Osteoarthritis focused on measuring Balneotherapy, Osteoarthritis

Eligibility Criteria

50 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Knee osteoarthritis with Kellgren and Lawrence stage 2 to 4 evidenced by a knee X-ray examination in the past 3 years); 100-normalized score of the WOMAC physical function subscale of 30 or greater; Available for balneotherapy program and the 6-month study follow-up; Signed inform consent; with health insurance affiliation. Exclusion Criteria: Presented with balneotherapy contra-indication; Having had spa treatment in the past 6 months or intra-articular corticosteroid injection within the previous 90 days or hyaluronic acid infiltration within the previous 6 months; Presented with chronic pain other than osteoarthritis, with scheduled surgery related to knee osteoarthritis; regulatory reason (guardianship or already enrolled in a clinical trial).

Sites / Locations

  • CEN

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

CONTROL

BALNEOTHERAPY PROGRAM

Arm Description

Standard of care for knee osteoarthritis

3-week balneotherapy program with Mineral Water of Saint Jean d'Angely in addition to standard of care for knee osteoarthritis

Outcomes

Primary Outcome Measures

Variation from baseline in physical function subscale of the WOMAC at 6 months
Physical function subscale of the Western Ontario and McMaster Universities Arthritis Index (WOMAC) is a self-administered questionnaire that consists in 17 items: (17 items): using stairs, rising from sitting, standing, bending, walking, getting in / out of a car, shopping, putting on / taking off socks, rising from bed, lying in bed, getting in / out of bath, sitting, getting on / off toilet, heavy domestic duties, light domestic duties. The 100-normalized subscale score ranges from 0 (none) to 100 (worse functional limitations).

Secondary Outcome Measures

Variation from baseline in physical function subscale of the WOMAC at 3 months
Physical function subscale of the Western Ontario and McMaster Universities Arthritis Index (WOMAC) is a self-administered questionnaire that consists in 17 items: (17 items): using stairs, rising from sitting, standing, bending, walking, getting in / out of a car, shopping, putting on / taking off socks, rising from bed, lying in bed, getting in / out of bath, sitting, getting on / off toilet, heavy domestic duties, light domestic duties. The 100-normalized subscale score ranges from 0 (none) to 100 (worse functional limitations).
Variation from baseline in pain subscale of the WOMAC at 3 months
Pain subscale of the WOMAC is a self-administered questionnaire that consists in 5 items: during walking, using stairs, in bed, sitting or lying, and standing upright. The 100-normalized subscale score ranges from 0 (none) to 100 (worse pain limitations).
Variation from baseline in pain subscale of the WOMAC at 6 months
Pain subscale of the WOMAC is a self-administered questionnaire that consists in 5 items: during walking, using stairs, in bed, sitting or lying, and standing upright. The 100-normalized subscale score ranges from 0 (none) to 100 (worse pain limitations).
Variation from baseline in stiffness subscale of the WOMAC at 3 months
Stiffness subscale of the WOMAC is a self-administered questionnaire that consists in 2 items: during walking, using stairs, in bed, sitting or lying, and standing upright. The 100-normalized subscale score ranges from 0 (none) to 100 (worse stiffness limitations).
Variation from baseline in stiffness subscale of the WOMAC at 6 months
Stiffness subscale of the WOMAC is a self-administered questionnaire that consists in 2 items: during walking, using stairs, in bed, sitting or lying, and standing upright. The 100-normalized subscale score ranges from 0 (none) to 100 (worse stiffness limitations).
Variation from baseline in WOMAC total score at 3 months
The scores for each subscale are summed up to calculate the total WOMAC score. The 100-normalized score ranges from 0 (none) to 100 (worse limitations).
Variation from baseline in WOMAC total score at 6 months
The scores for each subscale are summed up to calculate the total WOMAC score. The 100-normalized score ranges from 0 (none) to 100 (worse limitations).
Variation from baseline in pain-induced knee osteoarthritis intensity at 3 months
Pain intensity is measured using a 0 (no pain)-100 (Worse pain) Visual Analogic Scale (VAS).
Variation from baseline in pain-induced knee osteoarthritis intensity at 6 months
Pain intensity is measured using a 0 (no pain)-100 (Worse pain) Visual Analogic Scale (VAS).
Number of participants achieving minimal clinically important improvement (MCII) at 3 months
MCII is defined as 19.9 mm or greater on the VAS pain scale and/or 9.1 points or greater on the WOMAC physical function subscale normalized to a 0-100 score, and no knee surgery
Number of participants achieving minimal clinically important improvement (MCII) at 6 months
MCII is defined as 19.9 mm or greater on the VAS pain scale and/or 9.1 points or greater on the WOMAC physical function subscale normalized to a 0-100 score, and no knee surgery
Number of participants presented with acceptable symptom state (ASS) at 3 months
ASS is defined as VAS pain 32 mm or less or WOMAC function subscale normalized to a 0-100 score of 31 points or less.
Number of participants presented with acceptable symptom state (ASS) at 6 months
ASS is defined as VAS pain 32 mm or less or WOMAC function subscale normalized to a 0-100 score of 31 points or less.
Changes in participants quality of life at 3 months
Quality of life is measured using EUROQOL (EQ-5D-3L) questionnaire.The EQ-5D-3L descriptive system comprises the following five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 3 levels: no problems, some problems, and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results into a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state.
Changes in participants quality of life at 6 months
Quality of life is measured using EUROQOL (EQ-5D-3L) questionnaire.The EQ-5D-3L descriptive system comprises the following five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 3 levels: no problems, some problems, and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results into a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state.
Frequency of adverse events throughout the study
Adverse events are described using MedDRA and each event frequency is calculated.
Participants' opinion with their symptoms related to knee osteoarthritis at 6 months
Opinion is measured using a 5-point Likert scale

Full Information

First Posted
April 6, 2023
Last Updated
April 18, 2023
Sponsor
CEN Biotech
Collaborators
COMPAGNIE EUROPEENNE DES BAINS
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1. Study Identification

Unique Protocol Identification Number
NCT05819437
Brief Title
Knee Osteoarthritis and Balneotherapy
Acronym
ANGELLO
Official Title
Effectiveness of a 3-week Balneotherapy Program With Mineral Water of Saint Jean d'Angely in Knee Osteoarthritis: A Superiority, Randomised, Controlled Study Versus Standard of Care Alone
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
August 26, 2020 (Actual)
Primary Completion Date
July 3, 2021 (Actual)
Study Completion Date
September 20, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
CEN Biotech
Collaborators
COMPAGNIE EUROPEENNE DES BAINS

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
The goal of this clinical trial is to assess the efficacy of a 18-day balneotherapy program in the rheumatology indication in patients presented with knee osteoarthritis. The main questions of the study aims to answer are how balneotherapy improves functional incapacity and the disorders (pain, joint stiffness) induced by osteoarthritis of the knee, and thus improves patients' quality of life. Participants are randomly assigned in control or treatment (spa) groups. All receive standard of care for knee osteoarthritis throughout the study. Balneotherapy program consists of 18-days of spa treatment with Mineral Water of Saint Jean d'Angely. Functional incapacity, disorders and quality of life induced were measured at baseline and then 6 months later. Variation from baseline were compared in control and treatment groups to assess the efficacy of the balneotherapy program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
Balneotherapy, Osteoarthritis

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled Trial, monocentric
Masking
None (Open Label)
Allocation
Randomized
Enrollment
173 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CONTROL
Arm Type
No Intervention
Arm Description
Standard of care for knee osteoarthritis
Arm Title
BALNEOTHERAPY PROGRAM
Arm Type
Experimental
Arm Description
3-week balneotherapy program with Mineral Water of Saint Jean d'Angely in addition to standard of care for knee osteoarthritis
Intervention Type
Other
Intervention Name(s)
Balneotherapy program
Intervention Description
Whirlpool bath, bath with immersion showers, poultice application and underwater massage. The baths were performed in an individual tub in ten-minute sessions. The temperature was set specifically for each patient, on average from 34 to 38°C. These were baths with jets and air diffusion. The mud was applied as a poultice to the 2 knees and if necessary (duration of application: 10 minutes). The massages were carried out by qualified physiotherapists under an affusion ramp of thermal water at 38°C for 10 minutes. The water used is a mixed sulphated Natural Mineral Water, collected by drilling the "capuchins" at a depth of 975 m. The temperature of the water at the outlet of the borehole is 41.8°C and is lowered to 35°C.
Primary Outcome Measure Information:
Title
Variation from baseline in physical function subscale of the WOMAC at 6 months
Description
Physical function subscale of the Western Ontario and McMaster Universities Arthritis Index (WOMAC) is a self-administered questionnaire that consists in 17 items: (17 items): using stairs, rising from sitting, standing, bending, walking, getting in / out of a car, shopping, putting on / taking off socks, rising from bed, lying in bed, getting in / out of bath, sitting, getting on / off toilet, heavy domestic duties, light domestic duties. The 100-normalized subscale score ranges from 0 (none) to 100 (worse functional limitations).
Time Frame
Baseline (D1) and final (6 months)
Secondary Outcome Measure Information:
Title
Variation from baseline in physical function subscale of the WOMAC at 3 months
Description
Physical function subscale of the Western Ontario and McMaster Universities Arthritis Index (WOMAC) is a self-administered questionnaire that consists in 17 items: (17 items): using stairs, rising from sitting, standing, bending, walking, getting in / out of a car, shopping, putting on / taking off socks, rising from bed, lying in bed, getting in / out of bath, sitting, getting on / off toilet, heavy domestic duties, light domestic duties. The 100-normalized subscale score ranges from 0 (none) to 100 (worse functional limitations).
Time Frame
Baseline (D1) and final (3 months)
Title
Variation from baseline in pain subscale of the WOMAC at 3 months
Description
Pain subscale of the WOMAC is a self-administered questionnaire that consists in 5 items: during walking, using stairs, in bed, sitting or lying, and standing upright. The 100-normalized subscale score ranges from 0 (none) to 100 (worse pain limitations).
Time Frame
Baseline (D1) and final (3 months)
Title
Variation from baseline in pain subscale of the WOMAC at 6 months
Description
Pain subscale of the WOMAC is a self-administered questionnaire that consists in 5 items: during walking, using stairs, in bed, sitting or lying, and standing upright. The 100-normalized subscale score ranges from 0 (none) to 100 (worse pain limitations).
Time Frame
Baseline (D1) and final (6 months)
Title
Variation from baseline in stiffness subscale of the WOMAC at 3 months
Description
Stiffness subscale of the WOMAC is a self-administered questionnaire that consists in 2 items: during walking, using stairs, in bed, sitting or lying, and standing upright. The 100-normalized subscale score ranges from 0 (none) to 100 (worse stiffness limitations).
Time Frame
Baseline (D1) and final (3 months)
Title
Variation from baseline in stiffness subscale of the WOMAC at 6 months
Description
Stiffness subscale of the WOMAC is a self-administered questionnaire that consists in 2 items: during walking, using stairs, in bed, sitting or lying, and standing upright. The 100-normalized subscale score ranges from 0 (none) to 100 (worse stiffness limitations).
Time Frame
Baseline (D1) and final (6 months)
Title
Variation from baseline in WOMAC total score at 3 months
Description
The scores for each subscale are summed up to calculate the total WOMAC score. The 100-normalized score ranges from 0 (none) to 100 (worse limitations).
Time Frame
Baseline (D1) and final (3 months)
Title
Variation from baseline in WOMAC total score at 6 months
Description
The scores for each subscale are summed up to calculate the total WOMAC score. The 100-normalized score ranges from 0 (none) to 100 (worse limitations).
Time Frame
Baseline (D1) and final (6 months)
Title
Variation from baseline in pain-induced knee osteoarthritis intensity at 3 months
Description
Pain intensity is measured using a 0 (no pain)-100 (Worse pain) Visual Analogic Scale (VAS).
Time Frame
Baseline (D1) and final (3 months)
Title
Variation from baseline in pain-induced knee osteoarthritis intensity at 6 months
Description
Pain intensity is measured using a 0 (no pain)-100 (Worse pain) Visual Analogic Scale (VAS).
Time Frame
Baseline (D1) and final (6 months)
Title
Number of participants achieving minimal clinically important improvement (MCII) at 3 months
Description
MCII is defined as 19.9 mm or greater on the VAS pain scale and/or 9.1 points or greater on the WOMAC physical function subscale normalized to a 0-100 score, and no knee surgery
Time Frame
3 months
Title
Number of participants achieving minimal clinically important improvement (MCII) at 6 months
Description
MCII is defined as 19.9 mm or greater on the VAS pain scale and/or 9.1 points or greater on the WOMAC physical function subscale normalized to a 0-100 score, and no knee surgery
Time Frame
6 months
Title
Number of participants presented with acceptable symptom state (ASS) at 3 months
Description
ASS is defined as VAS pain 32 mm or less or WOMAC function subscale normalized to a 0-100 score of 31 points or less.
Time Frame
3 months
Title
Number of participants presented with acceptable symptom state (ASS) at 6 months
Description
ASS is defined as VAS pain 32 mm or less or WOMAC function subscale normalized to a 0-100 score of 31 points or less.
Time Frame
6 months
Title
Changes in participants quality of life at 3 months
Description
Quality of life is measured using EUROQOL (EQ-5D-3L) questionnaire.The EQ-5D-3L descriptive system comprises the following five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 3 levels: no problems, some problems, and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results into a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state.
Time Frame
3 months
Title
Changes in participants quality of life at 6 months
Description
Quality of life is measured using EUROQOL (EQ-5D-3L) questionnaire.The EQ-5D-3L descriptive system comprises the following five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 3 levels: no problems, some problems, and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results into a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state.
Time Frame
6 months
Title
Frequency of adverse events throughout the study
Description
Adverse events are described using MedDRA and each event frequency is calculated.
Time Frame
From inclusion to the final visit at 6 months
Title
Participants' opinion with their symptoms related to knee osteoarthritis at 6 months
Description
Opinion is measured using a 5-point Likert scale
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Knee osteoarthritis with Kellgren and Lawrence stage 2 to 4 evidenced by a knee X-ray examination in the past 3 years); 100-normalized score of the WOMAC physical function subscale of 30 or greater; Available for balneotherapy program and the 6-month study follow-up; Signed inform consent; with health insurance affiliation. Exclusion Criteria: Presented with balneotherapy contra-indication; Having had spa treatment in the past 6 months or intra-articular corticosteroid injection within the previous 90 days or hyaluronic acid infiltration within the previous 6 months; Presented with chronic pain other than osteoarthritis, with scheduled surgery related to knee osteoarthritis; regulatory reason (guardianship or already enrolled in a clinical trial).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arnaud TERRILLON-SEYTRE
Organizational Affiliation
CEN
Official's Role
Study Director
Facility Information:
Facility Name
CEN
City
Dijon
ZIP/Postal Code
21000
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

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Knee Osteoarthritis and Balneotherapy

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