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SOSteniamoci: An Internet-based Intervention to Support Informal Caregivers.

SOSteniamoci: An Internet-based Intervention to Support Informal Caregivers.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05301257
Enrollment
105
Registered
2022-03-29
Start date
2022-07-15
Completion date
2023-07-15
Last updated
2023-08-14

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

Conditions

Caregiver Burden

Keywords

informal caregiver, internet-based intervention, caregiver burden, culturally adapted, eHealth

Brief summary

The purpose of this study is to evaluate efficacy of internet intervention for informal caregivers in Italy in reducing their care-giving burden.

Detailed description

This intervention is going to take a form of an Internet-based Intervention (IBI) consisting of eight therapeutic modules. These are the themes, as listed chronologically: Introduction, Thoughts and Acceptance, Problem Solving, Stress and relaxation, Communication, Behavioural Activation, Worry and Anxiety, Maintenance. These themes were chosen after considering topics which might be the most useful for someone in a role of an informal caregiver, considering the trans-diagnostic nature of the intervention. Effect of the intervention will be compared against a wait-list control group. Intervention is in Italian.

Interventions

BEHAVIORALIntervention group SOSteniamoci

Intervention based on cognitive behavioural therapy principles and culturally adapted to Italian population. Intervention's main purpose is to reduce caregiver burden and increase quality of life. Intervention contains psycho-educational elements as well as examples and exercises.

Sponsors

Istituto Auxologico Italiano
CollaboratorOTHER
Linkoeping University
CollaboratorOTHER_GOV
Bar-Ilan University, Israel
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants will be randomly allocated to either control or intervention group. Participants in the control group will receive the same treatment once the intervention group is finished with the treatment.

Eligibility

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

Inclusion criteria

1. 18 years old or over and both gender; 2. spent at least the last couple of months providing care; 3. must have internet access and the ability to use a computer or any other compatible device; 4. must be able to complete a phone interview -

Exclusion criteria

1\) having severe physical or mental impairments, psychiatric conditions or neurological disorders; 2) the person in need of care has a life expectancy below or approximately around 6 months; 3) not able to use a computer or an electronic device; 4) not able to complete a phone interview; \-

Design outcomes

Primary

MeasureTime frameDescription
Cargiver Burden Inventory (CBI)Pre-treatment; Week 8; 12 months post-treatmentThis measure is used to evaluate caregiver burden. CBI contains 24 questions that are distributed within 5 facets - Time Dependency, Emotional Health, Development, Physical Health and Social Relationships. Answer options are presented on a 5-item Likert scale and ranges from from 0 ('Never') to 4 ('Nearly Always'). Total score on CBI is summed up and ranges from 0 to 96, higher score indicating higher levels of burden experienced.

Secondary

MeasureTime frameDescription
The Patient Health Questionnaire (PHQ-9)Pre-treatment; Week 8; 12 months post-treatmentMeasure will be used to evaluate depressive symptoms. It contains 9 questions that must be responded to by choosing an answer from 4-item Likert scale, where number 0 indicates 'Not at all' and 3 - 'Nearly every day'. Higher score indicates more severe symptoms.
Generalized Anxiety Disorder (GAD-7)Pre-treatment; Week 8; 12 months post-treatmentMeasure will be used to evaluate caregiver anxiety. GAD-7 contains 7 questions that must be responded to by choosing an answer from 4-item Likert scale, where number 0 indicates 'Not at all' and 3 - 'Nearly every day'. Higher score indicates more severe symptoms.
Perceived Stress Scale (PSS-10)Pre-treatment; Week 8; 12 months post-treatmentMeasure will be used to evaluate levels of experienced stress. It contains 10 questions on a Likert scale ranging from 0 ('Never') to 4 ('Very Often'). Higher score indicates more severe symptoms.
Couple Satisfaction Inventory (CSI-4)Pre-treatment; Week 8; 12 months post-treatmentThis questionnaire contains 4 statements regarding couple satisfaction. Each of the statements must be evaluated using a 6-item Likert scale. A higher score indicates higher couple satisfaction.
The Inclusion of Illness in the Self Scale (IIS) - Caregiver versionPre-treatment; Week 8; 12 months post-treatmentThis scale included a set of 7 pairs of concentric circles (one labeled 'Self' and one labeled 'Other's Illness') that vary in their degree of overlap from 1 (two separate circles) to 7 (almost completely overlapping circles).
World Health Organization (WHO-5)Pre-treatment; Week 8; 12 months post-treatmentThis questionnaire contains 5 statements regarding individual's well-being. Each of the statements must be evaluated using 6-item Likert scale with a score of 0 indicating 'At no time' while a score of 5 - 'All the time'. Higher score indicates higher well-being.

Countries

Italy

Outcome results

None listed

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