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Solution Focused Brief Therapy in the multicultural memory clinic: a mixed methods study

Solution Focused Brief Therapy in the multicultural memory clinic: a mixed methods study - TULIPA SFBT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON49748
Enrollment
200
Registered
2019-06-21
Start date
2019-07-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

dementia mild cognitive impairment

Interventions

One group receives five telephone sessions (45-60 minutes) of SFBT, while the other group receives care as usual.

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: * Patient and caregiver have visited the multicultural memory clinic; all diagnostic assessments (neuropsychological assessment, MRI etc.) have been completed * Patient was referred for cognitive complaints * Patient and caregiver are willing and able to give informed consent * Male or female, aged 18 years or above for caregivers, 30 years or above for patients.

Exclusion criteria

Exclusion criteria: * If severe psychiatric disorders requiring active treatment are present, as judged during the multidisciplinary meetings of the Alzheimer Center. * If the patient is unable to provide informed consent due to severe cognitive impairment, e.g. as shown by an inability to complete the screening measures of the neuropsychological assessment, or floor effects on more than one cognitive domain * If the patient is too impaired in speech or language comprehension to participate in the intervention, as judged by the investigator

Design outcomes

Primary

MeasureTime frame
The main study parameter is the group difference in the trajectories of quality of life from pre-, to directly post- and six months post-treatment.

Secondary

MeasureTime frame
The secondary study parameters are the group differences in the trajectories of depressive symptoms, solution focused skills and caregiver strain from pre-, to directly post- and six months post-treatment. Furthermore, we will perform a cost-effectiveness study.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)