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Family Talk Intervention in the Context of Specialised Palliative Home Care

The Family Talk Intervention in Clinical Practice When a Parent With Dependent Children is Severely Ill: An Effectiveness-implementation Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05365919
Enrollment
400
Registered
2022-05-09
Start date
2022-04-01
Completion date
2024-12-31
Last updated
2023-10-17

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

Conditions

Terminal Illness

Keywords

Specialised palliative care, Communication, Family Intervention

Brief summary

This intervention study aims to evaluate a psychosocial family based intervention in clinical practice, the Family Talk Intervention (FTI), for families with dependent children affected by life-threatening/life-limiting illness, when a parent is ill. The study has an effectiveness implementation hybrid design where both the effects of FTI and the implementation process in clinical practice are examined.

Detailed description

When a family with dependent children is affected by severe illness this affects the entire family. Still, there is little research evaluating support to such families. This intervention study aims to evaluate a psychosocial family based intervention in clinical practice, the Family Talk Intervention (FTI), for families with dependent children affected by life-threatening/life-limiting illness, when a parent is ill. The study has an effectiveness implementation hybrid design where both the effects of FTI and the implementation process in clinical practice are examined. FTI will be carried out as a cluster randomized trial at 12 clinics in specialized palliative homecare (6 units=intervention, 6 units=control). All social workers at these clinics will receive education and training in FTI in 2021. From 2022, FTI will be offered to families cared for at these care contexts. FTI is manual-based and consists of 6 meetings with the families (together and individually) and is led by the FTI-educated social workers. The aim of FTI are to support the family in talking about illness-related subjects (e.g. prognosis, stress), support parenting, and support the family in identifying their strengths and how to best use them. FTI will be evaluated through surveys and interviews with families before FTI/baseline and after completed intervention (3 and 6 months after baseline). Further, social workers will be invited to compete questionnaires and take part in focus groups about their experiences of FTI. The research group has conducted pilot-studies on FTI in these contexts with positive results. The present study allows us to take a further step in the evaluation of FTI- evaluate FTI under real conditions.

Interventions

FTI entails six meetings, with intervals of 1-2 weeks between meetings. Meetings 1-2 include only the parent(s) and focus on their experiences of the situation, as well as the consequences of the diagnosis for each family member. The parent(s) will formulate the goal of the intervention. Meeting 3: Interviews will be held with each child and includes the child's life situation. Meeting 4 includes the parent(s) and focuses on planning the family meeting. The children's thoughts and questions serve as a guide for the upcoming family meeting. Meeting 5 is a family meeting and consists of questions and issues raised earlier by the family members. Meeting 6 is a follow-up with all family members. The meeting is guided by the family members' needs, e.g., regarding communication and parenting. If the intervention is interrupted unexpectedly and cannot be finished as scheduled due to extraordinary circumstances, extra meetings are available (Meetings 7-11).

Sponsors

Forte
CollaboratorINDUSTRY
Ersta Sköndal University College
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

A cluster-randomized trial will be conducted at 12 homecare services (6 services=intervention, 6 services=control).

Eligibility

Sex/Gender
ALL
Age
6 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Families affected by a life-threatening or life-limiting illness and have dependent children, ill or health aged 0-19 years and * Enrolled in specialized palliative home care * At least two family members have accepted to participate

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Changes in family Communication over time. Family Adaptability and Cohesion Scale IVSix monthsMeasures in self-rated family communication which is the primary outcome of the intervention

Secondary

MeasureTime frameDescription
Changes in self-rated grief. Prolonged Grief Disorder (PG-12/PG-13).Six monthsAn instrument to screen for pathologic forms of grief before and after an expected death
Changes in self-rated anxiety. Generalized Anxiety Disorder (GAD)Six monthsMeasures symptoms of anxiety
Changes in The Strengths and Difficulties Questionnaire (SDQ)Six monthsMeasures self-rated strengths and difficulties. Has a proxy version for children
Changes in self-rated resilience. Resilience Scale (RS-14) ((Resilience Scale for Children (RS-10)).Six monthsMeasures self-rated resilience in adults and children
Changes in factors needed for successful implementation.The Swedish Normalization Process Theory Measure (S-NoMAD)Six monthsFor the implementation research. Characterizes and explains key mechanisms that promote and inhibit the implementation, embedding and integration of new health techniques, technologies and other complex interventions.
Changes in perception of organizational context. Alberta Context Tool (ACT)Six monthsFor the implementation research. Measures organizational context for use in complex healthcare settings.
Changes in self-perceived parenting skill. Parental Skills Checklist (PSC)Six monthsMeasures self-rated parenting abilities

Countries

Sweden

Contacts

Primary ContactMalin Lövgren, PhD
malin.lovgren@mchs.se+46766365090
Backup ContactAnette Alvariza, PhD
anette.alvariza@mchs.se+46766365073

Outcome results

None listed

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