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Development and Validation of Family Adjustment Inventory

Development and Validation of a New Instrument to Evaluate Parents' Adjustment to Their Child's Chronic Disease: the Family Adjustment Inventory

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04049890
Enrollment
900
Registered
2019-08-08
Start date
2016-03-15
Completion date
2026-09-14
Last updated
2025-02-17

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

Conditions

Adjustment Reaction

Keywords

adjustment, family functioning, chronic disease, emotions

Brief summary

A diagnosis of chronic disease in childhood may be disruptive for families. Some parents show good adjustment, while others may have more difficulties. Aim of this study is to develop and validate a new psychometric instrument to help precociously detect parents' vulnerability in the process of adjustment to their child's chronic disease at different times of care.

Detailed description

FAI was developed in two different forms: 1. for parents with one children suffering from a chronic disease or ill children who has siblings younger than 3 years old - FAI-O (only child); 2. for parents with at least two children, the brother/sister of the ill child has 3 years or more- FAS-S (siblings) The two forms are identical, with the exception that FAI-S has an additional dimension with respect to FAI-O, that specifically regards the involvement of siblings in the illness path of the sick brother/sister. Development of FAI followed several steps: * definition of initial instrument dimensions * item wording for each dimension * definition of scoring * focus group with parents of patients suffering from a chronic disease to evaluate item content and linguistic clarity Validation of FAI for each form (FAI-O and FAI-S): Validation consists in several steps, identical for the two versions but in different in timing, depending on the number of admnistration. * first phase: the FAI is administered to parents of patients with different chronic disease (each form needs to reach the total of 300 administrations). * second phase: statistical analysis aimed to obtain the final version of each FAI form (define actual dimensions and most adequate items) * third phase: administration to a new sample of parents of children suffering from a chronic disease (each form needs to reach the total of 150 administrations). * fourth phase: statistical analysis aimed to confirm the adequacy of the instrument

Interventions

OTHERFAI-O

Administration of Family Adjustment Inventory in the version Only-child

OTHERFAI-S

Administration of Family Adjustment Inventory in the version Sibling

OTHERPersonal Data Questionnaire

This form requires informations about child, respondent and partner (if any), and evaluates the presence of any distressful event happened during the last year

Sponsors

University of Florence
CollaboratorOTHER
Meyer Children's Hospital IRCCS
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* consent for participating in the study * having a child suffering from a chronic illness and treated in the hospital in the following specialties: onco-hematology, neuro-oncology, diabetology, cystic fibrosis, metabolic disease, gastroenterology, cardiology, nephrology, rheumatology, allergology, pneumology, immunology, intensive care unit * italian speaking

Exclusion criteria

* cognitive impairment * no good knowledge of italian language

Design outcomes

Primary

MeasureTime frameDescription
Perceived family adjustmentParents fill in the FAI one single time at enrollmentFAI (Family Adjustment Inventory) measures family adjustment. The preliminary versions of FAI-O consists in182 items and FAI-S in197 items, both scored on a 5-point likert scale from 0 to 4. Higher scores represent poorer adjustment.

Secondary

MeasureTime frameDescription
Presence of distressful events happened in the last yearParents fill in the personal data questionnaire one single time at enrollmentThe presence of distressful events is collected through a personal data questionnaire, specifically designed for this study in accordance to literature in the field

Countries

Italy

Contacts

Primary ContactRosanna Martin, MSc
rosanna.martin@meyer.it055 5662475
Backup ContactLaura Vagnoli, MSc
laura.vagnoli@meyer.it055 5662719

Outcome results

None listed

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