Acceptance and valued-living in palliative care patients, caregivers and significant others
- Conditions
- Depression and Prolonged GriefMental Health - DepressionMental Health - Other mental health disorders
- Registration Number
- ACTRN12614000150640
- Lead Sponsor
- niversity of Wollongong
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Stopped early
- Sex
- All
- Target Recruitment
- 460
Participants need to be aged 18 years or over and have sufficient comprehension of English to be able to understand and complete the study documents. Caregivers are identified by the patient as the primary informal caregiver; that is, the person who spends most time with the patient, who provides most of their informal day-to-day care, assistance and support. Significant others are identified by the patient or caregiver as a significant other who provides informal care, assistance or support and is perceived as being substantially affected by the patient’s situation.
Individuals with active psychosis, intellectual disability, moderate to severe cognitive impairment, or insufficient comprehension of English that would impair their ability to give informed consent and provide valid responses.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Acceptance (also known in the negative as experiential avoidance), measured by the Acceptance and Action Questionnaire - II [Pretreatment, 1 month posttreatment, 6 months postbereavement]
- Secondary Outcome Measures
Name Time Method Depression, measured by the Hospital Anxiety and Depression Scale [Pretreatment, 1 month posttreatment, 6 months postbereavement];Prolonged Grief, measured by the Prolonged Grief - 12 (preloss) and Prolonged Grief - 13 (postloss)[Pretreatment, 1 month posttreatment, 6 months postbereavement];Valued-living, measured by the Valued Living Questionnaire[Pretreatment, 1 month posttreatment, 6 months postbereavement]