Bilzen Hoeselt

This research aims to evaluate how a music and video-based group exercise therapy affects motivation, physical function, cognition, and well-being in older adults living with moderate dementia. The study focuses on participants aged 65 and older who experience moderate dementia and reside in nursing homes. The trial is designed to explore whether this therapy can improve various aspects of health and daily functioning in this population. Participants in the intervention group will join small group exercise sessions twice weekly for four months. During these sessions, they will watch a video of an older woman performing exercises on a large screen and will be encouraged to copy the movements. Each session lasts up to 45 minutes, and participants can select the music they prefer at the start of each session. The control group will continue their usual physical therapy without receiving the additional music and video-based therapy. Throughout the study, researchers will measure changes in motivation, muscle strength, compliance, adherence, and attrition rates at various points from baseline through four months. They will also assess balance, gait, activity levels, sleep, cognition, quality of life, and behavioral symptoms using established tests and questionnaires. Participants will be monitored during the intervention period, and evaluations will occur at baseline, mid-intervention, and study end to capture the therapys impact.

Researchers are evaluating the Suicidal Crisis Intervention SCI as a new short-term treatment method for people after a suicidal crisis or suicide attempt. This study aims to determine if SCI can reduce suicidality and also explore its effect on related factors such as hopelessness, defeat, entrapment, and interpersonal needs. The SCI was developed to provide evidence-based care in Flanders, addressing the limited interventions currently available for this high-risk group. The study compares two groups one receiving the SCI alongside their usual treatment, and the other receiving only their usual treatment. The SCI includes four sessions focusing on providing insight into suicidal crises, involving loved ones, creating a safety plan, and ensuring continuity of care. It emphasizes a structured, person-centered approach and aims to motivate participants toward specialized care. Participants will be followed for approximately 222 days after randomization. Researchers will assess changes in suicidality using the Beck Scale for Suicide Ideation at multiple points, along with secondary measures such as suicidal behavior, hopelessness, defeat, entrapment, isolation, follow-up care readiness, and treatment satisfaction. Assessments are conducted at baseline, 42 days, 132 days, and 222 days to monitor progress and outcomes throughout the study period.

Researchers are collecting detailed data about suicide attempts and suicidal thoughts among people who come to healthcare services in Flanders. The study aims to understand how often these behaviors occur, the methods used, and how many receive proper follow-up care after a suicide attempt. This observational study uses a structured interview tool called the Guideline for Suicide Care and Evaluation LOES to gather comprehensive information. Participants undergo a two-part semi-structured interview administered by trained nurses, psychologists, or psychiatrists. The first part happens soon after admission to a healthcare facility and collects information on emotional state, mental health history, social support, hopelessness, and suicidal behavior. The second part provides a deeper evaluation of risk factors, treatment needs, motivations, planning, and coping strategies related to suicidality. Throughout the study, participants provide demographic, clinical, and psychological information through interviews. Researchers assess suicidal intent, planning, past behavior, substance use risk, and care needs. The study tracks treatment agreements and care pathways after assessment. Data collection occurs at the initial presentation, with no drug or medical treatment being tested. The total participation time varies depending on the individuals healthcare encounters and follow-up.