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Long-term Consequences of Bereavement in Children, Adolescents and Young Adults

Bereavement in Children, Adolescents and Young Adults. - A Study of Health and Psychosocial Well-being in Adults Who Have Experienced Early Parental Death

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01453699
Enrollment
1225660
Registered
2011-10-18
Start date
2009-09-30
Completion date
2012-11-30
Last updated
2014-08-12

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

Conditions

Bereavement

Keywords

Bereavement, early parental death, grief, affective disorders, depression, depressive symptoms, socioeconomic factors, suicide, attempted suicide, antidepressive agents, cardiovascular diseases, quality of life, Long-term health effects, Socioeconomic outcomes, Psychosocial well-being

Brief summary

The purpose of this study is to examine how the death of a parent as a child, adolescent or young adult affects health and psychosocial wellbeing in adult life and to evaluate the impact in adult life of counseling to children, adolescents and young adults who lost a parent.

Detailed description

Early parental death experienced by 4% of the children in Western countries, is considered to be the most stressful and potentially harmful childhood life event and the health consequences may depend on the nature of the bereavement (e.g. relationship with bereaved), as well as by interpersonal (e.g. social support), intrapersonal (e.g. age and genetics), appraisal and coping factors. Studies have shown that children and adolescents have a greater risk of getting a psychiatric diagnose as well as psychological and social problems. Despite of the obvious consequences of losing a parent, there is a lack of systematic studies on the consequences later in life as well as studies that evaluate the counseling possibilities the children and adolescents are offered. The study will investigate: 1. Long-term health effects of experiencing parental death as a child adolescent or young adult. Focus will be on psychiatric outcomes including depression, severe cardiovascular disease, suicide, suicide attempts, psychological well-being and health related behavior. 2. Long term effects of experiencing parental death as a child, adolescent or young adult on socioeconomic outcomes as education, employment, marital status/ cohabitation status and number of children/age when having children. 3. The long-term psychosocial and behavioral impact of psychological intervention programmes to children, adolescents and young adults who have experienced the death of a parent. Focus will be on: Depressive symptoms, quality of life, posttraumatic stress disorder, life style, relationship functioning, grief and spirituality. A nationwide register based cohort of people born in Denmark will be established. Long-term health effects and socioeconomic outcomes of experiencing parental death will be based on nationwide clinical and administrative registries. Exposure is defined as experiencing the death of a parent before age 30. The long-term psychosocial and behavioral impact of psychological intervention programmes will be based on a combination of questionnaire data and data from registries. The part of the study using data from registries will be based on the nationwide cohort. The questionnaire based part of the study will include 3 groups selected from the nationwide cohort: 1. Persons who have lost a parent and participated in intervention programmes (identified through counseling centers), 2. Persons who have lost a parent, and not participated in intervention programmes (randomly selected matched on age and gender) and 3. Persons who have not lost a parent (randomly selected matched on age and gender). An invitation letter will be send to the 3 groups (5500 persons) by mail, and they will be asked to complete one questionnaire online.

Interventions

None listed

Sponsors

Statens Serum Institut
CollaboratorOTHER
Center for Crisis Psychology
CollaboratorUNKNOWN
Counselling and Research Center for Grieving Children, Teens and Young Adults
CollaboratorUNKNOWN
Children´s Welfare
CollaboratorUNKNOWN
Danish Cancer Society
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* persons born in Denmark

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Depressive symptomsParticipants will be answering the questionnaire once (not at a specifik age but between 18-40 years)The Center for Epidemiological Studies Depression Scale (CES-C)
Quality of lifeParticipants will be answering the questionnaire once (not at a specifik age but between 18-40 years)SF-36, Self-reported questionnaire
Complicated griefParticipants will be answering the questionnaire once (not at a specifik age but between 18-40 years)Inventory of Complicated Grief/ Prolonged Grief Disorder (PG-13) and Centrality of Event Scale, Self-reported questionnaire
PTSDParticipants will be answering the questionnaire once (not at a specifik age but between 18-40 years)Harvard Trauma Questionnaire (HTQ), Self-reported questionnaire
ExistentialityParticipants will be answering the questionnaire once (not at a specifik age but between 18-40 years)Posttraumatic Growth Inventory (PTGI, Self-reported questionnaire
Hospitalization for affective disorderPaticipants will be followed from age 15 until date of first hospitalization for an affective disorder, death, first emigration or end of follow up, an expected average of 12 yearsDanish Psychiatric Central Register
Use of antidepressive medicationPaticipants will be followed from age 20 until date of second independantly prescription of antidepressive medication, death, first emigration or end of follow up, an expected average of 9 yearsThe Danish National Prescription Registry
SuicidePaticipants will be followed from age 18 until date of suicide, other causes of death, first emigration or end of follow up, an expected average of 15 yearsDanish Register of Causes of Death
Severe cardiovascular diseasePaticipants will be followed from age 18 until date of first hospitalization for severe cardiovascular disease, death, first emigration or end of follow up, an expected average of 15 yearsThe Danish National Patient Register
Education levelParticipants will be followed from age 18 until highest attained educational level, death, first emigration or end of follow up, an average of 20 yearsThe Register-based System of Demographics and Social Statistics in Denmark
EmploymentEmployment status at age 30, death, first emigration or end of follow-up, an expected average of 8 years.The Register-based System of Demographics and Social Statistics in Denmark

Secondary

MeasureTime frameDescription
Support when losing a parentParticipants will be answering the questionnaire once (not at a specifik age but between 18-40 years)Self-report items
Lifestyle (smoking, alcohol, exercise)Participants will be answering the questionnaire once (not at a specifik age but between 18-40 years)Self-reported questionnaire
CopingParticipants will be answering the questionnaire once (not at a specifik age but between 18-40 years)Brief cope, Self-reported questionnaire
Relationship functioningParticipants will be answering the questionnaire once (not at a specifik age but between 18-40 years)Quality of relationship and intimacy, Self-reported questionnaire

Countries

Denmark

Outcome results

None listed

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