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Quality of Life and Psychosocial Dimension in Children With Hypopituitarism

Quality of Life and Psychosocial Dimensions in Children With Congenital or Acquired Hypopituitarism

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05403255
Acronym
QALHYPO
Enrollment
120
Registered
2022-06-03
Start date
2022-07-01
Completion date
2024-01-01
Last updated
2022-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital or Acquired Hypopituitarism

Brief summary

Relatively little is known about the quality of life (QOL) of patients with hypopituitarism, particularly children. Quality of life studies have mostly focused on improvements following the initiation of growth hormone treatment in adults with growth hormone deficiency. Overall QOL data on patients with multiple pituitary hormone deficiency or another isolated deficiency are much scarcer. These studies suggest however that pituitary deficiencies affect the QOL and social integration of adults. In children, the psychosocial repercussions of the disease are very poorly understood, particularly in the case of multiple congenital pituitary hormone deficiency.

Detailed description

Objectives: * Describe the quality of life and psychosocial repercussions of the disease in children 10-17 years of age with multiple pituitary hormone deficiency (either acquired or congenital), or isolated pituitary hormone deficiency (other than idiopathic isolated growth hormone deficiency). * Compare the QOL and psychosocial indicators of these patients with those of the general population * Study the effects of various factors (medical, social, psychological) on patient outcomes and experiences of the disease. Methods * Prospective analytical pilot study involving the four hospitals in the Referral Centre for Rare Pituitary Diseases (Centre de Référence des Maladies Rares de l'Hypophyse, HYPO) * Questionnaire data will be collected among patients and their parents during follow-up consultations. * Children's quality of life will be evaluated using the Kidscreen-10 questionnaire (for children and parents) and PedsQL multidimensional fatigue scale. Psychosocial indicators (standard of living, schooling, recreation activities, social and family relationships, perceived health status and physical appearance) will be gathered using a questionnaire based on the HBSC (Health Behaviour in School-Aged Children) questionnaire (INPES 2010), and compared with data from the general population of elementary-, middle-and high-school children in France.

Interventions

OTHERevaluation of the quality of life with questionnaires

Questionnaire data will be collected among patients and their parents during follow-up consultations. Children's quality of life will be evaluated using the Kidscreen-10 questionnaire (for children and parents) and PedsQL multidimensional fatigue scale. Psychosocial indicators (standard of living, schooling, recreation activities, social and family relationships, perceived health status and physical appearance) will be gathered using a questionnaire based on the HBSC (Health Behaviour in School-Aged Children) questionnaire (INPES 2010), and compared with data from the general population of elementary-, middle-and high-school children in France.

Sponsors

Assistance Publique Hopitaux De Marseille
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
10 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Age 10-17 years * Multiple or isolated pituitary hormone deficiency * Deficiency diagnosed for a least 6 months

Exclusion criteria

* Isolated growth hormone deficiency with normal MRI findings and/or no previous irradiation of the hypothalamo-pituitary region and/or no known genetic cause. * Secondary pituitary deficiency due to a secreting adenoma * Inability to complete the questionnaire (intellectual disability, low French language proficiency) * No health coverage

Design outcomes

Primary

MeasureTime frameDescription
Quality of life measurement1 dayThe KIDSCREEN-10 score consists of 10 items and provides a Rasch-scaled single score of HRQoL. Both self-report and proxy versions will be used.

Secondary

MeasureTime frameDescription
Psychosocial parameters1 dayHBSC questionnaires (Aged Behaviour in School-agedd Children, INPES 2014). This international standard questionnaire enables the collection of common data across participating countries and thus enables the quantification of patterns of key health behaviours, health indicators and contextual variables.
Socioeconomic status1 dayENVU questionaire ( Social and health vulnerability identification questionnaire in pediatrics )
Fatigue1 dayPedsQL multidimensional fatigue scale

Countries

France

Contacts

Primary ContactSarah CASTETS, PH
sarah.castets@ap-hm.fr04 91 38 67 30

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026