None listed
Conditions
Brief summary
This study entitled 'Kia ora ai te Iwi' emphasises the potential of ‘living well’ (a quality life worth living) and flourishing despite the collective adversity faced when impacted by mate wareware (dementia). The study design was developed in response to kaupapa Maori research conducted in the mental health and neurological sectors highlighting the need for access to cultural-specific psychological therapy for Maori embracing a ‘whole of whanau’ approach. The overarching aim of this study is to develop a robust, evidence-based, culturally-specific therapeutic Whanau oranga (‘whole whanau’ wellbeing) framework designed to enhance resilience and wellbeing amongst Maori impacted by mate wareware. This will be achieved through three key objectives: 1. To develop an effective culturally-specific therapeutic approach for Maori whanau impacted by mate wareware. The Whanau oranga approach will incorporate culturally adapted evidence-based psychological interventions within a kaupapa Maori healing framework. 2. To implement a pilot of the Whanau oranga approach with Maori whanau impacted by mate wareware in the Ngati Awa rohe. 3. To evaluate the Whanau oranga approach with Maori impacted by mate wareware in the Ngati Awa rohe (Whakatane Maori tribal area in New Zealand).
Interventions
A culturally-adapted evidence-based psychological program will be implemented and evaluated with Maori impacted by Dementia. Participants include primary caregivers and relatives of those diagnosed with this neurodegenerative condition. Specific interventions will include cognitive behavioural therapy (CBT) culturally adapted for Maori 'Poutama Hinetore' (Bennett, 2012), distress tolerance skills, mindfulness, and emotion regulation skills delivered within a kaupapa Maori framework incorporating tikanga Maori (Maori cultural practices) and te reo Maori (Maori language). Physical information used will include summary notes and diagrams following sessions supporting specifically related to new skills learnt. These sessions notes will be made available online for participants also. The materials will be culturally adapted CBT thought records (Beck, 2011) and (Dialectical Behavioural Therapy (DBT) skills worksheets (Linehan, 2014). Relevant Maori proverbs (whakatauki), myths and legends will be incorporated into this content. The intervention/therapy will be developed based upon the needs of the family and individual. This will be assessed using the Meihana model, a Maori clinical assessment tool that incorporates a holistic understanding of wellbeing. Specific therapies may include: CBT (processing grief, loss and negative emotions), DBT skills sessions, and mindfulness (including Maori modulation skills drawing upon traditional skills such as kapa haka (Maori cultural dance and song)). The intervention will be delivered by the lead investigator who is an experienced registered clinical psychologist. She is of Maori descent and accesses both clinical and cultural supervision. A rangahau whanau (research advisory group) will also provide oversight. The intervention will be delivered as group/family and individual sessions. This will be determined by the participants. The intervention will be delivered fortnightly over a 4 month period. This may be extended by 1-2 months should the need arise from participants. For example, if whanau require additional support. The decision would be made by the lead clinical psychologist in consultation with clinical supervision. The intervention will be implemented in a private environment of the participants choice. This may include their home, a marae (Maori cultural place of meeting), or an alternative space provided by the researcher. The intervention is not intended to be a manualised treatment intervention. The intervention, like therapy, will be determined based upon the needs of the participants.
Sponsors
Study design
Eligibility
Inclusion criteria
Maori living in the Ngati Awa region (Whakatane Maori tribe in New Zealand) impacted by Dementia, that is, living with the diagnosis of dementia and/or family members who are primary care-givers.
Exclusion criteria
Participants unable to provide informed consent, or access consent from their parent and/or guardian.