- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02552784
Quality of Life of Patients and Theirs Parents With Inherited Metabolic Diseases With Restricted Diet (MHMRSQol)
Determinants of Health Status and Quality of Life of Patients and Their Parents With Inherited Metabolic Diseases Diagnosed During Childhood and Requiring Restrictive and Specific Diet
Study Overview
Status
Detailed Description
The study 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 .
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.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Brigitte CHABROL
- Phone Number: 04 91 32 45 17
- Email: brigitte.chabrol@ap-hm.fr
Study Locations
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-
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Marseille, France, 13354
- Recruiting
- Hôpital de la Timone Assistance Publique Hôpitaux de Marseille
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Contact:
- Brigitte CHABROL
- Phone Number: 04 91 32 45 17
- Email: brigitte.chabrol@ap-hm.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Included in MHMRS databases from different centers
- 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.
Exclusion Criteria:
- Can't be included subjects not complying with at least one of the inclusion criteria previously mentioned .
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: 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 .
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient's anxiety assessment
Time Frame: 6 years
|
Anxiety assessment of children by autoquestionnaires: STAI-C (8-10 years old); STAI-Y (11-17 years old); STAI (patients becoming adults)
|
6 years
|
Assessment of adaptive coping strategies of patients
Time Frame: 6 years
|
Assessment of adaptive coping strategies of patients by questionnaires (BriefCope for adults patients, Kidcope for young patients)
|
6 years
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Patient's behavior assessment
Time Frame: 6 years
|
Assessment of child's behavior by Strengths and difficulties questionnaires and assessment of adult's behavior by the sociale adaptation scale (Weintraub scale)
|
6 years
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Patient's quality of life assessment
Time Frame: 6 years
|
Patient's quality of life assessment by VSP-A questionnaire
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6 years
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Parent's quality of life assessment
Time Frame: 6 years
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Parent's quality of life assessment by WHOQOL-BREF questionnaire
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6 years
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Assessment of adaptive coping strategies of parents
Time Frame: 6 years
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Assessment of adaptive coping strategies of parents by BriefCope questionnaire
|
6 years
|
Parent's anxiety assessment
Time Frame: 6 years
|
Parent's anxiety assessment by STAI questionnaire
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6 years
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2014-38
- 2014-A01874-43 (Registry Identifier: Ansm)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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