Informations générales (source: ClinicalTrials.gov)
Pedometers and Walking Tests for Pulmonary Hypertension Patients: a First, Prospective Psychology and Concordance Study (HTAPODO)
Interventional
N/A
University Hospital, Montpellier (Voir sur ClinicalTrials)
mars 2019
juin 2024
29 juin 2024
Concordance between walking tests and pedometer data may seem like a logical outcome for
pulmonary hypertension (PH) patients. However, many individuals have discordant results:
results much worse or better during an in-hospital walking test as compared to real life
activity.
The primary objective of this study is: to determine variables associated with
discordance between the distance walked during an in-hospital 6-minute walking test
(6MWT) and the average distance travelled per day (observed over a period of 28 days (2 ×
14 days) using a pedometer) among PH patients.
Etablissements
| Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| Arnaud de Villeneuve Hospital - 34295 - Montpellier - France | Contact (sur clinicalTrials) | ||||
Critères
Tous
Inclusion Criteria:
- Patient with idiopathic pulmonary hypertension (PH), familial PH, or PH associated
with various pathologies (groups I to IV of the international classification)
- New York Heart Association (NYHA) severity classes II to IV
- Incident cases, or prevalent cases with stable disease over the last 3 months
- Collection of informed written consent
- Affiliation with or beneficiary of a social security program (health insurance)
- Outpatient consulting at the hospital on the day of inclusion
- 6 minute walking test on day of inclusion
- Patient with idiopathic pulmonary hypertension (PH), familial PH, or PH associated
with various pathologies (groups I to IV of the international classification)
- New York Heart Association (NYHA) severity classes II to IV
- Incident cases, or prevalent cases with stable disease over the last 3 months
- Collection of informed written consent
- Affiliation with or beneficiary of a social security program (health insurance)
- Outpatient consulting at the hospital on the day of inclusion
- 6 minute walking test on day of inclusion
- Patients protected or unable to give consent according to Article L1121-8 of the
French Public Health Code (CSP)
- Pregnant or lactating women according to article L1121-5 of the CSP
- Vulnerable persons according to article L1121-6 of the CSP
- Simultaneous participation in any other research protocol
- It is impossible to correctly inform the patient (language barrier, etc.)
- The patient has already been included in the study