- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03015428
"Living Together With Dementia"_Creation and Validation of a Training Program for Family Caregivers of People With Dementia to Live at Home
Study Overview
Detailed Description
This study will begin in March 2016, with the initial assessment of family caregivers of people with dementia.
These were recruited through hospital neurology clinic and must comply with a set of pre-established criteria.
It is expected a total of 20 participants in the study (10 in the experimental group and 10 in control group).
Interventions will take place over the months of March and April. The final evaluation is scheduled for late April and the follow up to July 2016.
an evaluation document itself for this study was built.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Oporto, Portugal
- CHSaoJoao
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Be primary caregiver of the person with dementia
- Be able to read and write
- Carers of peolpe with dementia in initial or moderate stage
Exclusion Criteria:
- The person with dementia have severe mental pathologies associated
Study Plan
How is the study designed?
Design Details
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Psychoeducation
Interventions: Give information Teach and train strategies |
Providing knowledge and skills development in family caregivers of people with dementia, through a structured psychoeducational programme
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Caregiver Overload Scale
Time Frame: 7 weeks
|
7 weeks
|
|
Carers Assessment Satisfaction Index
Time Frame: 7 weeks
|
7 weeks
|
|
Carers Assessment Difficulties Index
Time Frame: 7 weeks
|
7 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Lia Sousa, Master, Centro Hospitalar de São João, E.P.E.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- LTWD1
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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