Quality of Life of Patients and Theirs Parents With Inherited Metabolic Diseases With Restricted Diet
NCT ID: NCT02552784
Last Updated: 2021-09-17
Study Results
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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UNKNOWN
NA
763 participants
INTERVENTIONAL
2015-01-31
2022-12-31
Brief Summary
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Detailed Description
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The evaluations include all data collected by querying patients and their families and medical data collected by the medical team.
The data collected concern in one hand explanatory variables characterizing the state of health and quality of life of patients, on the other variables describing the factors considered as potential determinants, namely:
* Socio -demographic and socio-economic on the patient and family.
* Clinical and therapeutic relative to the patient : age at the time of diagnosis, illness and consequences, type of treatment and diet.
* On possible alterations of physical health: overall assessment of the importance of using health professionals and specific description of the various physical health problems.
* Psycho- behavioral and cognitive.
* Quality of life of patients and their family.
* On the patient's relationship with the care system (access to care and satisfaction).
The frequency of evaluations is 2 years. The evaluation will be at a consultation in the usual medical monitoring way up conducted in these children, allowing to collect clinical information directly nearby medical teams that support them.
The various measurement tools used are:
* STAI-C and STAI-Y
* BRIEFCOPE and KIDCOPE
* GOODMAN questionnaire
* FAS questionnaire
* WECHSLER scale
* VSPA, VSPA-e and VSPA-p
* QUALIN
* WHOQOL-BREF
The project is under the authority of a Steering Committee comprising representatives of all the partners in the project teams. The project is supervised by the Scientific Council of the SFEIM (Société Francaise pour les Erreurs Inées du Métabolisme) and the G2M (Groupement des centres de référence et de compétence des Maladies héréditaires du Métabolisme) which is consulted on the scientific guidance of the project.
At the end of a study report will be prepared. It will detail all the decisions inherent in the conduct of the project and the results obtained. This report will be sent to the Ministry of Health under the cover of the Delegation for Clinical Research. The report will form the basis of the adjacent communications will be co-signed by the members of the Steering Committee and will reference the origin of the aid received.
Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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patients and their parents with inherited metabolic diseases
The population is a dynamic/open cohort consists of all patients MHMRS diagnosed and supported in one of the six Centers of Reference for Metabolical disease or one of the three Centers of Competence for Hereditary Metabolic Diseases or in the Center of Réference for Hereditary liver Metabolism Diseases since 2000. For each patient, the date of entry into the cohort is the diagnostic date of MHMRS. The study includes all prevalent and incident cases .
data assessment of the state of health and quality of life of patients and their families
Study medical determinants, socioeconomic, behavioral, environmental of health, school and professional integration, and short- and medium-term quality of life of all patients residing in France for which the diagnosis of hereditary diseases metabolism with specific diet (MHMRS) was performed during their childhood.
Interventions
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data assessment of the state of health and quality of life of patients and their families
Study medical determinants, socioeconomic, behavioral, environmental of health, school and professional integration, and short- and medium-term quality of life of all patients residing in France for which the diagnosis of hereditary diseases metabolism with specific diet (MHMRS) was performed during their childhood.
Eligibility Criteria
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Inclusion Criteria
* Age less than 18 years at diagnosis
* Diagnostic MHMRS made from 01/01/2000
* Treatment and management of MHMRS initiated in one of the clinical sites
* Living in France
* Living
* Compliance with criteria for inclusion in the cohort
* Having agreed to participate in the study
* Allowed to participate in the study by the parents or legal guardians for any minor subject.
* Excludes all subjects at least one of the following criteria:
* Moving outside France after baseline ( initial treatment performed in one of the participating centers )
* Withdrawal of consent / refusal of monitoring;
* Not responding at three successive waves of investigation.
17 Years
ALL
No
Sponsors
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Assistance Publique Hopitaux De Marseille
OTHER
Responsible Party
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Principal Investigators
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Urielle DESALBRES
Role: STUDY_DIRECTOR
Assistance Publique Hôpitaux de Marseille
Locations
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Hôpital de la Timone Assistance Publique Hôpitaux de Marseille
Marseille, , France
Countries
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Central Contacts
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Facility Contacts
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References
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Ouattara A, Resseguier N, Cano A, De Lonlay P, Arnoux JB, Brassier A, Schiff M, Pichard S, Fabre A, Hoebeke C, Guffon N, Fouilhoux A, Broue P, Touati G, Dobbelaere D, Mention K, Labarthe F, Tardieu M, De Parscau L, Feillet F, Bonnemains C, Kuster A, Labrune P, Barth M, Damaj L, Lamireau D, Berbis J, Auquier P, Chabrol B. Individual and Family Determinants for Quality of Life in Parents of Children with Inborn Errors of Metabolism Requiring a Restricted Diet: A Multilevel Analysis Approach. J Pediatr. 2023 Mar;254:39-47.e4. doi: 10.1016/j.jpeds.2022.08.060. Epub 2022 Oct 17.
Other Identifiers
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2014-A01874-43
Identifier Type: REGISTRY
Identifier Source: secondary_id
2014-38
Identifier Type: -
Identifier Source: org_study_id
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