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Families Experiencing Cancer - Support to Prevent Cancer-related Illness

Families Experiencing Cancer - Support to Prevent Cancer-related Illness

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07390019
Acronym
FamCASP
Enrollment
800
Registered
2026-02-05
Start date
2026-02-02
Completion date
2032-12-30
Last updated
2026-02-05

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

Conditions

Cancer, Family Members, Support, Family

Brief summary

In this planned project, we aim to evaluate the FamCASP model and the digital screening tool SCa-N as an intervention within routine cancer care. An expected outcome of FamCASP is an increase in family health as expressed in lower levels of psychological distress, improved coping strategies and family climate and a decrease in unmet needs as measured by family members' self-reports as well as their descriptions during interviews. Hence, the specific aims are to: I. Describe differences in psychological distress, coping strategies, family climate and unmet needs between baseline and follow-up in family members receiving support according to the FamCASP model in outpatient cancer clinics and to explore whether or not there are differences between family members receiving support and those who do not receive support. II. Describe family members' experiences of receiving support according to the FamCASP model. III. Describe family members' experiences of interacting with the digital tool.

Interventions

OTHERFamCASP

Support model

Sponsors

Malmö University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Cluster

Eligibility

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

Inclusion criteria

Participants are adult (≥18years) family members to patients diagnosed with CRC. Inclusion criteria are the ability to read and understand Swedish and having access to a computer, tablet or mobile phone to access the digital screening tool as well as the study information.

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Support needs12 months post diagnosisThe Supportive Care Needs Survey - Partners and Caregivers

Secondary

MeasureTime frameDescription
Health12 months post diagnosisEQ5D

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026