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Interaction at the end of life in dyads of parents and adult children

Interaction at the end of life in dyads of parents and adult children - Dy@EoL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00013206
Enrollment
48
Registered
2017-10-27
Start date
2018-02-22
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Terminally ill adult children who receive palliative and/or hospice care and their parents as well as terminally ill parents who receive palliative and/or hospice care and their adult children

Interventions

Group 1: Patients and relatives are interviewed once via face-to-face qualitative semi-strcutured in-depth interviews and assessed via quantitatvie self-report questionnaires.

Sponsors

Medizinische Hochschule Hannover, Institut für Allgemeinmedizin und Palliativmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria comprise for dyad A) terminally ill patients 18 years of age or older who are seeking palliative or hospice care and who are in contact with at least one living parent and for dyad B) terminally ill parents who are seeking palliative or hospice care and who are in contact with at least one child age 18 years or older. Dyads of parents and children related through adoption or fosterage will be included. Having received comprehensive oral and written information about the nature, the content and aim of the study and about study participation, both patient and family member/s provide written informed consent in order to be eligible to participate as a dyad in this project. If the terminally ill patient is not available to participate in the study, but agrees that the project team contacts an eligible relative for study participation, this relative will be offered study participation. If one of the dyad partners refuses to participate in the study or withdraws consent before, during or after the study, the already collected data of the respective dyad partner may be used in the study or the planned data collection can take place respectively. Individuals of both sexes and all ethnic backgrounds independent of their main diagnosis may participate in the study.

Exclusion criteria

Exclusion criteria: Exclusion criteria include (1) significant emotional distress during interview, (2) cognitive impairment such as dementia, (3) non-proficiency in German, (4) patient and/or family member does not consent to participate in the study.

Design outcomes

Primary

MeasureTime frame
Qualitative and quantitative overview of characteristics of interaction of both dyads The qualitative overview is obtained by one-time semi-structured in-depth interviews and the quantitative overview is obtained from questionnaires. The following questionnaires are used: 1) demographic questionnaire, 2) Relationship-specific Attachment Scales for Adults, 3) Berlin Social Support Scales, and 4) Graphic Closeness Scale.

Countries

Germany

Contacts

Public ContactFranziska A. Herbst

Medizinische Hochschule Hannover, Institut für Allgemeinmedizin und Palliativmedizin

herbst.franziska@mh-hannover.de+49 511 532-4991

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 6, 2026