Family

9

Review clinical trials related to Family. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Connecting Today to Combat Social Isolation and Loneliness

The investigators developed Connecting Today, a feasible and highly acceptable remote visiting program that can support care home residents living with moderate to severe dementia to have video calls with their family members, friends, or care partners. The investigators will recruit 80 residents from 4 care homes, and their family members, friends, or care partners. All participants will be offered 60 minutes of Connecting Today per week for 6 weeks (in either the intervention group, or in the wait-list control group). An onsite care provider will be trained to tailor the video calls, and facilitate positive verbal and non-verbal engagement during the calls. The investigators will evaluate how Connecting Today affects outcomes for residents (quality of life, loneliness, and responsive behaviours) and their remote visitors (quality of life, loneliness, and social support). The investigators will assess how outcomes differ for men, women, and people with different perceptions and experiences of Connecting Today.

Participants needed: 320
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: University of AlbertaUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

are at least 65 years old [+7]

All remote visitors are required to understand and speak English as this is nece...

Status: Recruiting

Families Implementing Good Health Traditions for Life

This study will provide evidence for the utility of using a community-engaged research approach to implement a tailored, family-oriented adaptation of the Diabetes Prevention Program that will have positive effects on risk factors associated with type 2 diabetes morbidity and mortality among Black families in a Southwest Georgia community.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Morehouse School of MedicineUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Family 1.a.) Black Parent/Guardian: age 18 years or older residing in the same h... [+3]

Individuals with severe psychological disorders that may prevent/interfere with... [+6]

Status: Recruiting

K-ORCA: Testing a Decision Support Tool and Group Process for Selecting Interventions

This proposal responds to NIMH Objective 4.2.c to develop "decision-support tools and technologies that increase the effectiveness and continuous improvement of mental health interventions" by leveraging the Family First Prevention Services Act (FFPSA) policy opportunity. First, a web-based platform to host (a) a decision-support tool and (b) automated facilitation for group decisions with the tool will be developed with state partners' feedback. Next, decision makers leading their states' FFPSA quality improvement efforts will be engaged to pilot a decision-support intervention comprised of the tool and live or automated facilitation, and to evaluate the implementation quality of evidence-based programs adopted with the decision-support intervention.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Chestnut Health SystemsUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

Non-institutionalized [+8]

Status: Recruiting

The Effectiveness of AIFIGA Program on Nursing Home Nursing Staff and Family and Residents'Health

This study aims to develop and evaluate the longitudinal effectiveness of the Artificial Intelligence Family Involvement Generative Agent (AIFIGA) program in enhancing the health of nursing staff, family, and residents' health through the use of a sequential, mixed methods research design. The development of a real-time, interactive, and informative AIFIGA program that sparks innovation is necessary to achieve effective communication between families and nursing staff. In Phase I, lasting 18 months, we will develop the AIFIGA program based on triangulate research design, observation and in-depth interview understanding the daily communication experiences and expectations from both families and nursing staff perception in Nursing Homes(NHs) after COVID-19, as well as our previous years' research results. The training data for AIFIGA will be derived from the collection of communication dialogues in these qualitative data. Furthermore, the intelligence of AIFIGA will be developed using publicly available large language models (LLMs). In Phase II, spanning the next 18 months, we will evaluate the longitudinal effects of the AIFIGA program on the health of residents, families, and nursing staff, tracking changes over time (baseline, 1 month, 3 months, and 6 months). There will be two groups of participants: (a) an AIFIGA group that receives the AIFIGA program and uses it for 3 months, and (b) a control group that receives only routine care.

Participants needed: 210
Trial details
Age: 20+Biological sex: AllType: InterventionalSponsor: Chang Gung Memorial HospitalUpdated: Feb 9, 2026Locations: 1
Eligibility criteria

residents aged ≥ 60 years, resident's family were aged equal or higher than 20 y... [+6]

Status: Recruiting

Effect of FPCA on Incidence of Emergency Delirium in Children After Surgery

Emergence delirium (ED) stands out as a prevalent postoperative complication among paediatric patients, correlating with extended hospitalization periods, escalated healthcare expenses, and increased incidence of postoperative maladaptive behaviours (POMBs). There is a lack of well-established pharmacological or non-pharmacological interventions demonstrating efficacy in reducing the occurrence of ED. Therefore, our objective is to assess the potential of family-centred perioperative care for anaesthesia (FPCA) in mitigating the incidence of ED in children, compared with routine anaesthesia.

Participants needed: 444
Trial details
Age: 2-6Biological sex: AllType: InterventionalSponsor: Second Affiliated Hospital of Wenzhou Medical UniversityUpdated: Dec 29, 2025Locations: 1
Eligibility criteria

Children aged 2-6 years undergoing elective surgery with an estimated surgical d... [+2]

Suffering important organ diseases; [+6]

Status: Recruiting

Family Involvement in ICU

The aim of this prospective cohort study was to investigate the effect of the time spent with relatives of patients treated in a tertiary intensive care unit on patient outcomes. The main question it aimed to answer was: Does spending more time with relatives of patients in intensive care result in lower sedative agent requirements? Does spending more time with relatives of patients in intensive care result in less delirium, fewer ventilator days, and shorter ICU stays?

Participants needed: 122
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Istanbul University - CerrahpasaUpdated: Jan 17, 2025Locations: 1
Eligibility criteria

Patients aged 18 and over. [+1]

Patients with pre-existing cognitive impairment or dementia. [+3]

Status: Recruiting

Family Centred Healthcare - Zero Separation and Couplet Care

Today mother and infant are routinely separated directly after birth if there is a need of specialised treatment and care, despite of the significant and positive effects of skin-to-skin contact. Thus, there is a need of change in organizing the treatment and care in a way that minimizes separation. The aim is to evaluate the implementation and effect of a complex family-centred intervention based 107 on zero separation and couplet care. The intervention is rooted in the philosophy of family-centred care. Essentially, mother infant dyads will be admitted together, where they will receive couplet care by neonatal nurses. The study comprises a quasi-experimental trial and a qualitative process evaluation including a field study and two interview studies. Finally, a health economic evaluation will be conducted to assess the cost-effectiveness of this complex intervention. The intervention will take place at the Neonatal Intensive Care Unit at Hvidovre Hospital. The nurses will as a part of the intervention be educated to take care of both mother and infant and carry out the intervention. Five families with experiences from the Neonatal Intensive Care Unit and the Maternity Unit participates as patient and public representative in the project, as their experiences and ideas will provide an added value to the project. This study contribute with a new perspective on how to organize the treatment and care of a newborn family in a Neonatal Intensive Care Unit. The study will be the first to examine zero separation and couplet care within sick mother-infant dyads. The study will provide knowledge about how an intervention consisting of zero separation and couplet care can be feasible and acceptable, and what kind of effect and impact it will provide. It is expected that the study as a whole may impact and profile clinical nursing, as well as benefitting public health.

Participants needed: 556
Trial details
Biological sex: AllType: InterventionalSponsor: Copenhagen University Hospital, HvidovreUpdated: Aug 21, 2024Locations: 1
Eligibility criteria

Mothers with a treatment-requiring condition such as preeclampsia, bleeding, psy... [+1]

Healthy mothers who does not need care and treatment, and has an infant admitted... [+1]

Status: Recruiting

Danish Diabetes Birth Registry 2

Pregnancies in women with pre-existing diabetes are considered "high risk" pregnancies, poses daily clinical challenges and in terms of research - a number of unanswered questions. Therefore, the investigators wish to establish a nationwide cohort of pregnancies complicated by pre-existing diabetes - the Danish Diabetes Birth Registry (DDBR2) The DDBR2 registry comprises all types of pre-existing diabetes including T1D, T2D and other types (as MODY), generating a nationwide cohort of mother/partner/children trios with accessible registry-, clinical data and biological biobank samples. This will enable the investigators to use data longitudinally to examine short- and long-term outcomes of pregnancies in women with diabetes.

Participants needed: 2,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Odense University HospitalUpdated: Apr 12, 2024Locations: 4Duration: 10 Months
Eligibility criteria

Women, age ≥ 18 years [+3]

No proficiency in Danish or English to understand oral and written information

Status: Recruiting

Efficacy of the Use of Diaries in Intensive Care Units

Randomized clinical trial that aims to evaluate the impact of the use of a diary in patients and relatives of patients admitted to an ICU in relation to usual practice in terms of health-related quality of life, the post-traumatic stress and anxiety/depression at 2, 6 and 12 months after ICU discharge.

Participants needed: 240
Trial details
Age: 18-100Biological sex: AllType: InterventionalSponsor: University of BarcelonaUpdated: Mar 27, 2024Locations: 1
Eligibility criteria

admitted intensive care unit [+4]

verbal manifestation of psychiatric, mental or cognitive antecedents [+1]