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Caregiver Stress Syndrome clinical trials

View clinical trials related to Caregiver Stress Syndrome.

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NCT ID: NCT06409455 Not yet recruiting - Clinical trials for Caregiver Stress Syndrome

Positive Dementia Caregiving: Clinical Trial of an Online Training Program

Start date: August 2024
Phase: Phase 2
Study type: Interventional

The goal of this study is to learn if a new online training program is helpful to dementia family caregivers. This online program is fully computerized and supports 24/7 access from any location. The main questions it aims to answer are: - Does the training program improves the participants' well-being and sense of positive meaning? - If the program is found to be helpful, does it work through enhancing caregivers' self-belief or getting them to practice positive interpretation of caregiving challenges? To answer these questions, researchers will compare the online program to a waitlist control. Participants will: - Use the intervention (requiring internet access) in a self-guided manner - Respond to brief questionnaires at the beginning, and 1, 2 and 3 months afterwards

NCT ID: NCT06357078 Recruiting - Clinical trials for Caregiver Stress Syndrome

Art Therapy and Caregivers Stress

Start date: January 2, 2024
Phase: N/A
Study type: Interventional

This research will be conducted to determine the effect of art therapy on the stress, anxiety and well-being of caregivers in the palliative care service.

NCT ID: NCT06307535 Recruiting - Caregiver Burden Clinical Trials

A Study of Meaning-Centered Psychotherapy for Caregivers to People With Cancer

Start date: February 29, 2024
Phase: Phase 3
Study type: Interventional

Participants will complete 1 set of questionnaires about 2 weeks before beginning their Meaning-Centered Psychotherapy for Caregivers/MCP-C or standard Supportive Psychotherapy for Caregivers/SP-C sessions. These questionnaires will ask about participants' sense of meaning and purpose in life, spiritual well-being, depression and/or anxiety, and social support. Participants will then be assigned to receive either MCP-C or SP-C for 7 sessions. Participants will complete additional sets of questionnaires about 2 weeks, 6 months, and 12 months after their last session of MCP-C or SP-C. It will take between 35 and 50 minutes to complete each set of questionnaires. After participants complete the MCP-C or SP-C sessions and all 4 sets of questionnaires, their participation in this study will end. If participants decide not to complete all 7 sessions, they may still choose to complete the questionnaires. Participants may remain in the study and continue to receive all 7 sessions of MCP-C or SP-C even if their loved one passes away.

NCT ID: NCT05992467 Active, not recruiting - Caregiver Burden Clinical Trials

WECARE: A Behavioral Intervention for Dementia Caregivers

WECARE
Start date: September 1, 2023
Phase: N/A
Study type: Interventional

This study aims to pilot test a culturally tailored behavioral intervention called "WECARE" to enhance caregiving mastery and improve psychosocial wellbeing of Chinese American family caregivers of persons with Alzheimer's Disease and related dementia.

NCT ID: NCT05927805 Not yet recruiting - Dementia Clinical Trials

E-bibliotherapy for Informal Caregivers of People With Dementia

Start date: September 2023
Phase: N/A
Study type: Interventional

The objective of this study is to test the efficacy of e-bibliotherapy on improving the psychological well-being of informal caregivers of people with dementia as compared with a control group.

NCT ID: NCT05547945 Recruiting - ADHD Clinical Trials

The Effects of Health Promotion Program for the Caregivers of Attention Deficit/Hyperactivity Disorders Children

Start date: May 19, 2018
Phase: N/A
Study type: Interventional

Objective: To explore the effect of health promotion programs on parental stress, quality of life, and health-promoting lifestyles for primary caregivers who had children with ADHD. Children's ADHD symptoms were also examined. Methods: A randomized control trial was conducted between July 2017 and April 2018. Primary caregivers aged 20 to 65 years who had ADHD children aged 7 to 12 years were recruited from a psychiatric outpatient department. Sixty caregivers were randomized to the health promotion group intervention (n=30) and the control groups (n=30). The control group received usual care. Study instruments included the Swanson, Nolan, Pelham, Version IV (SNAP-IV), Parenting Stress Scale (Short form), Taiwan's Concise World Health Organization Quality of Life Questionnaire (WHOQOL-BREF), and Health-Promotion Lifestyle Profile. Both groups were evaluated before and immediately after the intervention at 1, 3, and 6 months. GEE was applied for statistical analysis. Results: 60 participants were randomized to the health promotion intervention (n=30) or the control group (n=30). To explore the effect of health promotion programs on parental stress, quality of life, and health-promoting lifestyles for primary caregivers who are caring for children with ADHD. Conclusion: We hope that the Health promotion program could demonstrate the effect in reducing parental stress, improving the quality of life, promoting healthy lifestyles for primary caregivers, and reducing the symptoms of children with ADHD. Proper intervention programs should be incorporated in clinical practice settings in order to facilitate mental health well-being for caregivers of ADHD children.

NCT ID: NCT05465109 Recruiting - Caregiver Burden Clinical Trials

Traumatic Brain Injury and Alzheimer's Disease/Related Dementias Caregiver Support Intervention

TACSI
Start date: July 1, 2022
Phase: N/A
Study type: Interventional

The TBI-AD/ADRD Caregiver Support Intervention (TACSI) incorporates psychosocial and psychoeducational approaches with the objective of: a) identifying stressors associated with caregiving for family members who have the dual diagnosis of traumatic brain injury and dementia; and b) supporting caregivers in developing more effective coping and communication strategies as well as enhanced caregiving self-efficacy.

NCT ID: NCT05336344 Recruiting - Depression Clinical Trials

Supporting Family Caregivers of Persons With Dementia

ENCODE
Start date: July 15, 2022
Phase: N/A
Study type: Interventional

Based on preliminary work, whereby investigators examined pain management challenges and needs of caregivers of hospice patients with dementia, this team designed a cognitive behavioral intervention informed by the relational model of stress, entitled ENCODE (Empowering Caregivers of Patients with Dementia) to assist caregivers in effectively identifying and communicating their pain management challenges and needs. The investigators propose a 5-year randomized clinical trial in which caregivers of patients with Alzheimer's Disease and Related Dementias (ADRD) will be randomly assigned to a group receiving standard hospice care with the addition of "friendly video-calls" providing social support (attention control group) or a group receiving standard hospice care with the addition of the ENCODE intervention (intervention group).

NCT ID: NCT05195489 Active, not recruiting - Clinical trials for Caregiver Stress Syndrome

Examining the Impact of Family Connectors

Start date: March 7, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to understand the impact of Family Connectors, a peer-to-peer support and education program for family members who have participated in OnTrackNY, a treatment program for adolescents and young adults.

NCT ID: NCT05165186 Recruiting - Dementia Clinical Trials

Care Planning for a Loved One With Dementia: Knowledge, Preparing for Decisions, and Emotions

Start date: April 13, 2022
Phase: N/A
Study type: Interventional

The overall objective of this study is to compare knowledge, decisional conflict, preferences, and caregiver burden over time caregivers of Alzheimer's Disease and Related Dementias (ADRD) patients by comparing the effectiveness of a video decision aid intervention and enhanced usual care.