Foot Reflexology on Chronic Pain in Parkinsonian Patients

NCT ID: NCT04705207

Last Updated: 2023-08-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-04-14

Study Completion Date

2023-05-25

Brief Summary

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Pain is one of the non-motor symptoms of Parkinson's disease still poorly known and misdiagnosed and its management is complex. This encourage to explore new non-drug therapeutic paths, such as foot reflexology (FR). the present study proposed a comparison of the evolution of different parameters, quantitative and qualitative, to identify biomarkers and highlight the specific effect of FR on pain, compared to sham massage.

Detailed Description

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Parkinson's disease (PD) is a neurodegenerative disease characterized by the destruction of specific neurons population involved in movement control. Pain is one of the non-motor symptoms still poorly known and misdiagnosed. In addition to this fact, its management is complex. At present, the medical community has no effective solution to reduce pain to an acceptable level in terms of intensity or frequency.

Pain is a personal, subjective experience with an affective and cognitive dimension. The context and its psychological impact can amplify as well as alleviate the pain. Thus, non-pharmacological treatment (NPT) that influence the psychological state (mood, level of stress, ...) can also modulate the pain experience through the brain matrix of pain. Among them, foot reflexology, which by stimulating reflex zones located on the feet, makes it possible to modify the perception of the pain and to modify the subjective / emotional valence of the pain. In this study, we propose to evaluate this technique, by postulating that it should reduce the chronic pain of patients with Parkinson's disease.

This project is innovative and original in two dimensions : On the one hand, the pain of patients in PD is still often underestimated, there is in the mere fact of devoting a study a real dynamic of change in the consideration of the patients concerned and in the management of this non-motor symptom. On the other hand, the increasing use of NPT requires that clinical studies be conducted. To date, it is clear that very few or no reliable studies have been conducted on the subject. We wish to develop complementary non-pharmacological management to provide concrete help to Parkinson's patients and thus initiate the scientific validation of NPT as recommended by the High Authority of Health.

The study hypothesize that through a comparison of the evolution of different parameters, quantitative and qualitative, this study will allow to identify biomarkers and highlight the specific effect of FR on pain, compared to sham massage.

Conditions

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Parkinson Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

a group has intervention, a group has placebo intervention
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

DOUBLE

Participants Outcome Assessors
placebo is a traditional massage instead of a intervention reflexology massage

Study Groups

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reflexology massage

foot reflexology massage

Group Type EXPERIMENTAL

reflexology massage

Intervention Type PROCEDURE

the patient receive only foot reflexology massage

sham massage

traditional foot massage

Group Type PLACEBO_COMPARATOR

sham massage

Intervention Type PROCEDURE

the patient receive only foot traditional massage

Interventions

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reflexology massage

the patient receive only foot reflexology massage

Intervention Type PROCEDURE

sham massage

the patient receive only foot traditional massage

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patient with an age egal at 18 years old or more,
* Patient presenting a little fluctuating Parkinson's disease attested by a score ≤ 2 on the MDS UPDRS IV,
* Patients with chronic pain for at least 3 months with a VAS ≥ 4
* Patients whose anti-parkinsonian treatment is stable throughout the duration of the study and at least for 4 weeks.

Exclusion Criteria

* Patients with cognitive impairment defined by an MOCA\<25
* Patient presenting contraindication to carrying out the MRI examination
* Patient refusing to be informed of any abnormality detected on brain MRI
* Patient included in a clinical trial that potentially interferes with the objective of the study,
* Patient resistant to foot massage,
* Patient having benefited from a Foot reflexology session in the last 6 months, - Patient presenting skin lesions in the feet,
* Patient having a recent fracture in the feet,
* Patient having an history of phlebitis less than 3 months and history of deep vein thrombosis.
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Toulouse

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Christine BREFEL-COURBON, MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Toulouse

Locations

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University Hospital of Toulouse

Toulouse, , France

Site Status

Countries

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France

References

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Joineau K, Harroch E, Boussac M, Fabbri M, Leung C, Ory-Magne F, Rousseau V, Peran P, Brefel-Courbon C, Descamps E. Effect of foot reflexology on chronic pain in Parkinson's disease: A randomized controlled trial. PLoS One. 2025 Jul 28;20(7):e0327865. doi: 10.1371/journal.pone.0327865. eCollection 2025.

Reference Type DERIVED
PMID: 40720491 (View on PubMed)

Other Identifiers

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RC 31/20/0279

Identifier Type: -

Identifier Source: org_study_id

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