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Understanding hormone-related changes in Parkinson’s symptoms

Researchers want to help women with Parkinson’s identify and manage symptom changes linked to hormones, including changes around menstrual periods.

Testing a treatment or activity · Study reference: NCT06582212

Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓

Open the official registry record ↗

Who can join?

Ages 18 years to 56 years · Does not accept healthy volunteers

These are starting points, not the full rules. The research team can tell you whether the study is right for your situation.

Read all the rules for taking part

Sex eligibility reported by registry: female

Inclusion Criteria: * Non-menopausal women * Diagnosis of PD according to the MDS criteria onset of PD symptoms since at least two years before inclusion * Age 18-56 years * On stable medication regimen for PD for at least two months without foreseen need to modify it within the next three months * With and without OCP or intrauterine devices (IUD Exclusion Criteria: * Post-menopausal women with PD * Any condition that, in the opinion of the investigator, will preclude the participant from successfully or safely completing study procedures (i.e., dementia, severe depression, etc.) * People not able to give an informed consent.
Full study name & original research details

Official study title

Enabling Women With Parkinson's Disease to Identify and Better Manage Hormonal Triggers

Short title used by the registry

Enabling Women With Parkinson's Disease to Identify and Better Manage Hormonal Triggers of Parkinsonian Symptoms

Original description

Forty percent of people living worldwide with Parkinson's disease (PD) are women. Twenty percent of patients have PD onset under the age of 60 years, a time when women may encounter significant caregiving responsibilities along with occupational and other competing demands. Studies with surveys of women with PD (WwPD) have reported worsening of PDrelated symptoms especially in the week prior and the week of menses. However, prospective evidence is scarce and clinical guidelines to manage this issue do not exist. As a result, care is either non-existent or fragmented. The investigators propose a French multicentre prospective pilot study to capture changes in PD symptoms in relation to the stages of the menstrual cycle aiming at reducing hormonal related worsening in PD symptoms through neurologist intervention and/or patient selfmanagement. Digital technology will remotely enable patient reported outcome (PRO) tracking through the My Moves Matter app changes in PD symptoms during several months. This information will then help neurologists to customize treatment. Changes in motor symptoms will also be highlighted by tracking through the use of a wearable device (PDMonitor) to objectively detect motor changes together with the app. This will further support the reliability of the app. This study will provide evidence for the impact of the menstrual cycle on PD and help neurologists and patients to better manage PD symptoms related to these hormonal changes.

Further description from the registry

This is a prospective multicentre pilot study of the impact of the menstrual/hormonal cycle on PD symptoms and their treatment in pre-menopausal WwPD based on the remote tracking of PD symptoms and menstrual/hormonal cycle through the MMM digital health app in the French language. There is an ongoing European preliminary study investigating the usability of the MMM App to track menstrual symptoms in WwPD, endorsed by the Parkinson's Disease Research Cluster in the University College Cork in Ireland. The aim of that study does not overlap with the current proposal. The aims of the LADY-PD project are: 1. Aim 1. To determine the reliability of using our new mobile application to track motor and non-motor symptoms in pre-menopausal WwPD. French WwPD will use the My Moves Matter (MMM) application downloaded in their mobile phone to track their PD symptoms during their hormonal cycle. Changes during the cycle can be identified using a linear system to quantify changes in each symptom. The investigators will measure drop-out rate, missing data, usability, and acceptability (the latter with questionnaires for patients and neurologists). 2. Aim 2. To compare the mobile application subjective motor data against the gold standard clinical scale, the motor part of the Movement Disorders Society Unified Parkinson Disease Rating Scale (MDS-UPDRS). This will be done acquiring data coming from a subset of WwPD who will have an objective measurement of the MDS-UPDRS (using the PDMonitor, a digital device able to measure bradykinesia, tremor, gait, posture, rigidity, dyskinesia) while using the mobile application. Statistical analysis will compare data between the two devices. 3. Aim 3. To determine the clinical efficacy of interventions (changes on medication, physiotherapy, et cetera) suggested by the neurologists to improve motor and nonmotor symptoms detected by the mobile application during the initial 3-month period of evaluation. Effects of pharmacological and non-pharmacological interventions will be measured using the mobile app after a 3-month period of evaluation. The investigators hypothesize that 1. pre-menopausal WwPD will experience a worsening of motor and NMS during their menstrual/hormonal cycle (and possibly independently by OCP treatment); 2. these changes will have a relevant impact on the well-being of patients, and on their daily and social activities; 3. appropriate management of these changes can effectively improve quality of life of pre-menopausal WwPD.

Conditions reported: Digital Technology; Mobile Application; Motor Fluctuations; Oestrogen; Parkinson Disease

Study type
Interventional
Interventions
Mymovesmatter mobile application
Phases
NA
Sponsor
University Hospital, Grenoble
Start date reported by registry
2025-03-12 (actual)

Registry updated: 2026-10-02 · Status last verified by the registry submitter: 2026-09

Registry records retrieved 2026-10-11 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.

Contact the research team

Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.

Elena MORO · 0476769452 · emoro@chu-grenoble.fr

PIERRE PELISSIER · 0476769459 · ppelissier@chu-grenoble.fr

Study locations

Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.

CHU Grenoble Alpes

Grenoble, France

Recruiting

ELENA MORO · emoro@chu-grenoble.fr

Pierre PELISSIER · 0476769452 · ppelissier@chu-grenoble.fr

CHU Nantes Hôpital Laennec

Nantes, France

Recruiting

Philippe DAMIER, Pr · 33 (0)2.40.16.52.12 · philippe.damier@chu-nantes.fr

Régis FRENAIS · 33 (0)2 44 76 87 57 · regis.frenais@chu-nantes.fr

CHU Rennes -Site Pontchaillou

Rennes, France

Recruiting

Sophie DRAPIER, PH · +33 2 99 28 42 93 · Sophie.Drapier@chu-rennes.fr

Françoise KESTENS · 33 (0)2 99 28 93 34 · ide recherche neuro PPEV <ide.recherche.neuro.PPEV@chu-rennes.fr>

Chu Toulouse

Toulouse, France

Recruiting

Christine BREFEL-COURBON, PH · 33 (0)5 61 14 59 62 · christine.brefel-courbon@univ-tlse3.fr

Estelle HARROCH · +33 5 61 77 55 41 · harroch.e@chu-toulouse.fr

The original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.