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Social Isolation clinical trials

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NCT ID: NCT06467214 Not yet recruiting - Social Isolation Clinical Trials

Increasing Veterans' Social Engagement and Connectedness

CONNECTED
Start date: July 1, 2024
Phase: Early Phase 1
Study type: Interventional

Social isolation is a negative social determinant of health (SDoH) that affects 1-in-5 adults in the U.S. and 43% of Veterans. Social isolation is estimated to cost the nation $6.7 billion annually in federal healthcare spending. Yet, social isolation has rarely been the direct focus of healthcare interventions. The proposed project is a randomized controlled trial that seeks to test the effectiveness of the Increasing Veterans' Social Engagement and Connectedness (CONNECTED) intervention on social isolation among diverse Veteran groups in primary care clinics. CONNECTED involves three key services delivered by peers via telehealth through individual and group sessions over 8 weeks: 1) peer support, which includes person-centered assessment for social isolation, 2) psychosocial interventions to address social isolation, and 3) navigation (i.e., connecting Veterans to social resources). Findings from this study will contribute to the VA's efforts to address SDoH among Veterans and to provide high quality, person-centered, and equitable care to all Veterans.

NCT ID: NCT06458335 Not yet recruiting - Opioid Use Disorder Clinical Trials

Opioids and Loneliness

Start date: July 1, 2024
Phase: N/A
Study type: Interventional

This study aims to enroll 300 participants who will be assigned to one of three 3 groups. Each group will receive an intervention lasting 6, weekly sessions of 40-60 minutes. Eligibility include having an opioid use disorder and reporting loneliness or feeling alone or disconnected.

NCT ID: NCT06405620 Not yet recruiting - Social Isolation Clinical Trials

Use of a Social Assistance Robot in a Population of Children Subjected to Prolonged Isolation

BUDDY-GUARD
Start date: June 1, 2024
Phase: N/A
Study type: Interventional

During the period of isolation of the hospitalized child, contacts between the child and his family are impaired. Being away from home as well as from the social and family circle can be harmful for the hospitalized child. It seems necessary to measure the impact of the use of such an assistance robot both on the user himself and his family. Thus, it seems relevant to scientifically validate the benefit of using such an assistance robot to break iatrogenic social isolation and to measure the impact of this use.

NCT ID: NCT05031247 Not yet recruiting - Social Isolation Clinical Trials

Refugee Mental Health and Wellness Pilot Study

Start date: September 2022
Phase: N/A
Study type: Interventional

This pilot study will develop and examine the acceptability of a Community Navigator program of support for 10-24 older adult Arab Americans participants receiving services at a refugee-serving organization based in Southern California. This program will provide participants with social support from a 'Community Navigator,' who will work with clients to help promote attendance and engagement with the community during social activities and community events. This program aims to reduce feelings of loneliness or social isolation. In partnership with the refugee-serving organization, the UCLA investigators will implement this program in addition to services provided as usual at the community partner site. Researchers will then conduct interviews to explore participants' experiences and perceptions for improvement of the program.

NCT ID: NCT04840420 Not yet recruiting - Social Isolation Clinical Trials

An Effectiveness-implementation Hybrid Study of Social Prescribing in a Singapore Community Hospital Setting

Start date: April 19, 2021
Phase: N/A
Study type: Interventional

This research is an effectiveness-implementation hybrid study with two aims: 1) to determine the utility of a WBC (Well Being Coordinator)-driven Social Prescribing model in the intermediate care setting; and 2) to assess the patient health outcomes associated with the implementation pilot. The implementation research questions include: 1. Practical fit: Does the intervention fit with the daily life activities of study participants? What is the level of safety and burdensomeness of the frequency, intensity and duration of the intervention? 2. Acceptability: What are the acceptance, retention and follow-up rates as the participants move through the intervention? What are the reasons for retention? 3. Adoption: How well do the WBC carry out the assessment and intervention as planned? The key hypotheses include: 1. Participants in the intervention group will incur a higher improvement in perceived general wellbeing and social support than those participants in the control group. 2. Participants in the intervention group will incur less healthcare utilisation than those in the control group. 3. Improvement in the perceived general wellbeing and social support will be moderated by the level of social support of participants.

NCT ID: NCT04392115 Not yet recruiting - Social Isolation Clinical Trials

The PREPARE for COVID Trial

Start date: June 15, 2020
Phase: N/A
Study type: Interventional

This is a randomized trial of home-based exercises versus control for older adults during the COVID-19 pandemic. The hypothesis is that participation in a home-based program will reduce the risk of adverse effects of physical distancing by decreasing patient-reported disability, improving mental health and avoiding hospitalization or institutionalization for vulnerable older people

NCT ID: NCT04346940 Not yet recruiting - Social Isolation Clinical Trials

The Effectiveness of Telerehabilitation-Based Exercises in Elderly People

Start date: August 10, 2020
Phase: N/A
Study type: Interventional

An epidemic of pneumonia , which is thought to have developed due to a new coronavirus, was detected in Wuhan, Hubei Province of the People's Republic of China, and this epidemic could not be brought under control, leading to other provinces of China in a short time and then to a pandemic. It has spread all over the world including the European continent. Causative Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2) and the disease caused by the new virus (novel) coronavirus-2019 (2019-nCoV) and subsequently the COVID-19. After the virus was officially detected in our country on 11 March 2020, the number of cases increased rapidly and the virus was isolated in 670 patients within 10 days. The group that is most affected by the outbreak and has the highest mortality rate is the elderly with known cardiovascular diseases. It is important to ensure the social isolation of elderly patients and to minimize all hospital applications as much as possible if they do not have life-threatening urgent problems. To this end, Turkey on 21 March 2020, 65 years of age and older people and patients with chronic curfew was implemented. Individuals moving away from social life are dealing with their body more, their level of depression and anxiety increase, and their physical functions decrease. The therapy service is offered to people who cannot travel with telerehabilitation, which is defined as the transmission of rehabilitation service to long distances by using electronic information and communication technology. The purpose of this study is to investigate the effects of telerehabilitation exercises given to elderly individuals on sleep quality, quality of life and balance within the scope of geriatric rehabilitation.