Psychological Concomitants of Morquio Syndrome (The MAP Study)
NCT ID: NCT01752296
Last Updated: 2013-12-04
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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COMPLETED
20 participants
OBSERVATIONAL
2012-07-31
2013-10-31
Brief Summary
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It is well established in the health psychology literature, however, that the interaction between our physical health and our psychological health is bidirectional; that is, just as our physical health affects us emotionally (e.g. chronic pain can contribute to depression), so can our psychological health affect us physically (e.g. anxiety can contribute to feelings of chest pain). It is thus critically important to pay attention to the emotional and psychological symptoms associated with all lysosomal storage diseases, including Morquio, and expand our treatment standard of care to include mental health treatment, if necessary.
The first step in understanding and treating psychological conditions in Morquio disease is determining the natural occurrence of psychological symptoms in this population in comparison with non-medical populations. As little has been done in this regard, a pilot study documenting the occurrence rate of psychological issues and overall quality of life in patients with Morquio is the first item in order and will be the focus of this study.
Approximately 20 patients with Morquio disease will be invited to participate, recruited through Emory's Lysosomal Storage Disease Center, as well as through attendance at Morquio support groups and relevant regional, national and/or international meetings. Once consented, patients will be asked to complete three different self-report questionnaires, including the Achenbach System of Empirically Based Assessment (ASEBA) Adult Self-Report (ASR) or Older Adult Self-Report (OASR) questionnaire, the Short Form 36-item Health Questionnaire (SF-36), and the Brief Pain Inventory (BPI). Group aggregate data only will be reported; individual questionnaire content and results will be held confidential, except as in accordance with Georgia law relating to reporting of child or elder abuse, suicidal and/or homicidal intent. Completion of these questionnaires will complete subjects' participation in this pilot study.
Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
2. Patient is at least 18 years old.
3. Patient is not currently receiving enzyme replacement therapy for MPS IV.
4. Patient must provide written, informed consent prior to study participation.
Exclusion Criteria
2. Previous hematopoietic stem-cell transplant
3. Patient has a clinically significant disease (with the exception of symptoms of Morquio), including clinically significant immunologic, pulmonary, neurologic, or renal disease, or other medical condition, serious intercurrent illness, or extenuating circumstances that, in the opinion of the investigator, would confound the effects of Morquio upon study variables
18 Years
ALL
No
Sponsors
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BioMarin Pharmaceutical
INDUSTRY
Nadia Ali, PhD
OTHER
Responsible Party
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Nadia Ali, PhD
Health Psychologist / Instructor
Principal Investigators
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Nadia Ali, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Emory University
Locations
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Emory University
Decatur, Georgia, United States
Countries
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Other Identifiers
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BioMarin-1
Identifier Type: OTHER
Identifier Source: secondary_id
IRB00058524
Identifier Type: -
Identifier Source: org_study_id