Development and Validation of Family Adjustment Inventory
- Conditions
- Adjustment Reaction
- Interventions
- Other: FAI-OOther: FAI-SOther: Personal Data Questionnaire
- Registration Number
- NCT04049890
- Lead Sponsor
- Meyer Children's Hospital IRCCS
- 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
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 900
- 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
- cognitive impairment
- no good knowledge of italian language
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Parents of children with a chronic disease with no siblings FAI-O Parents of children suffering from a chronic disease who has no brother or sister over 3 years of age Parents of children with a chronic disease with siblings Personal Data Questionnaire Parents of children suffering from a chronic disease who one or more sibling over the age of 3 years old Parents of children with a chronic disease with siblings FAI-S Parents of children suffering from a chronic disease who one or more sibling over the age of 3 years old Parents of children with a chronic disease with no siblings Personal Data Questionnaire Parents of children suffering from a chronic disease who has no brother or sister over 3 years of age
- Primary Outcome Measures
Name Time Method Perceived family adjustment Parents fill in the FAI one single time at enrollment FAI (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 Outcome Measures
Name Time Method Presence of distressful events happened in the last year Parents fill in the personal data questionnaire one single time at enrollment The presence of distressful events is collected through a personal data questionnaire, specifically designed for this study in accordance to literature in the field
Trial Locations
- Locations (1)
Meyer Children's Hospital
🇮🇹Firenze, Italy