- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05797571
SOSteniamoci: Stakeholders' Survey
March 30, 2023 updated by: Istituto Auxologico Italiano
Informal Caregivers and Clinicians' Knowledge, Awareness, Attitude and Expect Barriers Towards Internet-based Interventions: A Stakeholders' Survey in Italy
Informal care is defined as the unpaid care provided to an older, frail, or ill person, by a person such as a spouse, a parent, a child, another relative, a neighbor, or a friend.
This phenomenon may lead to stress, burden, and decreased informal caregivers' quality of life.
Since lack of time, distance from services, and financial strains make the provision of psychological interventions to informal caregivers often challenging, Internet-based (self-help) programs might represent a viable solution to promote their emotional well-being.
Still, despite the proven benefits of internet-based intervention, no available programs for informal caregivers are available for the Italian population.
Nevertheless, planning and developing an online intervention, involving possible stakeholders (caregivers), might facilitate the understanding and dissemination of, willingness to use, and success of the future intervention.
Thus, the goal of the current study is to assess Italian stakeholders' knowledge about, awareness of, attitudes towards, willingness to participate and use, and expected barriers to internet-based interventions.
Study Overview
Status
Completed
Conditions
Detailed Description
The present study assessed the knowledge and awareness, attitudes, willingness to participate in, and expected barriers towards using Internet-based interventions to alleviate caregivers' burden in a sample of Italian caregivers and clinicians.
To this aim, an online stakeholders' survey was conducted in Italy among clinicians and informal caregivers, using a snowballing sampling technique.
Participants were asked to fill in the informed consent and complete the online survey as a clinician, a caregiver, or both.
Data were monitored daily.
Descriptive statistics and Pearson correlation analysis were used for data analysis.
Study Type
Observational
Enrollment (Actual)
150
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Milan, Italy, 20145
- Giada Pietrabissa
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Formal and informal caregivers
Description
Inclusion Criteria:
- clinicians and informal caregivers
- aged 18 years or older
- internet access
- basic computer literacy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Mean score in Online survey for clinicians
Time Frame: At baseline, during online survey, performed after signing informed consent
|
Online survey for clinicians - 30 items
|
At baseline, during online survey, performed after signing informed consent
|
Mean score in Online survey for informal caregivers
Time Frame: At baseline, during online survey, performed after signing informed consent
|
Online survey for informal caregivers - 45 items
|
At baseline, during online survey, performed after signing informed consent
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Giada Pietrabissa, PhD, Istituto Auxologico Italiano
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 15, 2022
Primary Completion (Actual)
December 15, 2022
Study Completion (Actual)
December 15, 2022
Study Registration Dates
First Submitted
March 13, 2023
First Submitted That Met QC Criteria
March 30, 2023
First Posted (Actual)
April 4, 2023
Study Record Updates
Last Update Posted (Actual)
April 4, 2023
Last Update Submitted That Met QC Criteria
March 30, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 03C212
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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