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Family Caregivers clinical trials

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NCT ID: NCT03587974 Completed - Family Caregivers Clinical Trials

Randomized Controlled Trial to Test an Alzheimer's Family Caregiver Intervention in Vietnam

Start date: June 10, 2018
Phase: N/A
Study type: Interventional

This is a cluster randomized controlled trial to determine the feasibility and preliminary effectiveness of culturally adapted psychosocial intervention for Alzheimer's family caregivers in Vietnam. The psychosocial intervention is being compared with an enhance control condition.

NCT ID: NCT03565757 Completed - Advanced Cancer Clinical Trials

Stress Management and Resilience Training (SMART) Intervention for Family Caregivers of Individuals With Advanced Cancer

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

This study examines Stress Management and Resilience Training (SMART) for family caregivers (FCG) of patients receiving chemotherapy for advanced cancer to potentially help with the stressful aspects of providing care. All participants will receive the SMART intervention.

NCT ID: NCT03397667 Completed - Quality of Life Clinical Trials

The Aging Brain ANSWERS Program

ABC ANSWERS
Start date: August 1, 2018
Phase: N/A
Study type: Interventional

This study will test the effectiveness of an intervention for Veterans diagnosed with Alzheimer's Disease (AD) or Traumatic Brain Injury (TBI) and the burden on their informal (family/friend) caregiver.

NCT ID: NCT03301831 Completed - Depressive Symptoms Clinical Trials

Resourcefulness Intervention With Parents of Technology-Dependent Children

Start date: February 5, 2018
Phase: N/A
Study type: Interventional

Technology-dependent children, those who live at home but rely on medical equipment such as mechanical ventilation or feeding tubes, require complex care for their chronic condition. Parents usually provide a majority of their care and are often overwhelmed by the caregiving demands resulting in deterioration of their own mental and physical health. The goal of this 2-arm (intervention vs. attention control) RCT is to test a cognitive-behavioral Resourcefulness Training intervention that includes teaching social (help-seeking) and personal (self-help) resourcefulness skills; ongoing access to video vignettes of caregivers of technology-dependent children describing resourcefulness skill application in daily life; 4 weeks of skills' reinforcement using daily journal writing; weekly phone calls for the first 4 weeks; and booster sessions at 2 and 4 months post enrollment. The intervention is proposed to improve these caregivers' mental and physical health outcomes and family functioning outcomes while they continue to provide vital care for these vulnerable children.

NCT ID: NCT02616107 Completed - Family Caregivers Clinical Trials

Improving Cancer Family Caregivers' Knowledge and Communication About Care Options

Start date: July 2014
Phase: N/A
Study type: Interventional

The purpose of this two-year mixed methods study is to develop and test an intervention to improve cancer family caregivers' knowledge of care options (curative, palliative, and hospice care) and goals of care communication as part of a self-management (SM) training program. The two specific aims of this project are to: 1. Develop a psycho-educational intervention called Managing Cancer Care: A Caregiver's Guide (MCC-CG), for family caregivers of patients with breast cancer to increase knowledge of care options, goals of care communication, and other SM skills. 2. Evaluate the feasibility and preliminary efficacy of the MCC-CG in a pilot randomized controlled trial compared with an attention-control condition (symptom management education) on knowledge of care options, goals of care communication, and other key SM skills (engagement in SM, management of transitions and uncertainty, increasing self-efficacy, appropriate use of health care resources).

NCT ID: NCT02580461 Completed - Family Caregivers Clinical Trials

Renewing Caregiver Health and Well-being Through Exercise

RECHARGE
Start date: June 2015
Phase: N/A
Study type: Interventional

The RECHARGE study is evaluating the effect of a 24 week structured exercise and education program on the physical and emotion health, quality of life, physical activity and fitness levels of family caregivers. Very little research has been done examining the impact of a structured exercise program designed for family caregivers of cancer patients. The purpose of this study is to determine if physical activity is effective in improving caregiver health and well-being.

NCT ID: NCT02283437 Completed - Family Caregivers Clinical Trials

A Problem-solving Based Bibliotherapy Program for Family Caregivers in Schizophrenia

PSBPF
Start date: April 1, 2018
Phase: N/A
Study type: Interventional

This proposed randomized controlled trial will test the effectiveness of a problem-solving based bibliotherapy program (PSBPF) for Chinese family caregivers in schizophrenia spectrum disorders. A repeated-measures, three-group design will be used to evaluate and compare the effects between two treatment groups (PSBPF and behavioral management group) and routine outpatient service (control group) for 150 randomly selected family caregivers of outpatients with schizophrenia-spectrum disorders over a 18-month follow-up.

NCT ID: NCT02211092 Completed - Family Caregivers Clinical Trials

Feasibility Study of a Home-based Physical Activity Intervention for Family Caregivers of People With Advanced Cancer

Start date: November 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to develop an individually tailored home-based physical activity intervention for family caregivers of people with advanced cancer and assess the feasibility of a future randomized controlled trial (RCT) to test the effects of this intervention.

NCT ID: NCT01468857 Completed - Stress Clinical Trials

Physical and Emotional Health of Caregivers for People Who Have Had Stem Cell Transplants

Start date: September 26, 2011
Phase:
Study type: Observational

Background: - Stem cell transplants are a complex treatment that can have serious side effects. Having a caregiver to help with the recovery is critical. Serving in this role, however, can cause high stress levels and negative health effects. Researchers want to better understand the health effects of caring for a family member or friend after a stem cell transplant. Understanding these effects can help develop programs that support caregivers coping with the demands of post-transplant care. Objectives: - To study the physical and emotional health of caregivers for a family member or friend who has had a stem cell transplant. Eligibility: - Individuals at least 18 years of age who are planning to be a caregiver for a person having a stem cell transplant. - Healthy non-caregiver volunteers for comparison studies. Design: - A caregiver will be caring for a transplant recipient just before transplant admission and up through 6 weeks after hospital discharge. The caregiver will usually live with or spend at least 6 hours each day with the recipient. - All participants will have three study visits. The first visit will happen before the transplant. The second and third visits will happen at the recipient s discharge, and 6 weeks after discharge. The following tests will be done at each visit: - A health assessment with a physical exam and review of life events and current health problems - Blood, hair, and saliva samples - Questionnaires about stress levels, personal health, and the caregiving process. - Caregiver participants may have an optional fourth study visit within 72 hours after an ICU admission. This visit will include the same tests as the other visits....

NCT ID: NCT01275495 Completed - Stroke Clinical Trials

Telephone Assessment and Skill-Building Intervention for Stroke Caregivers

TASKII
Start date: May 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the efficacy of the revised Telephone Assessment and Skill-Building Kit (TASK II) compared with an Information, Support, and Referral (ISR) intervention in family caregivers of stroke survivors. We will also test if TASK II intervention effects on primary outcomes (depressive symptoms, caregiving-related negative life changes, unhealthy days) are mediated through effects on secondary outcomes (task difficulty, optimism, threat appraisal). Comparative costs and outcomes for the TASK II and ISR interventions will also be explored.