Social Functioning

8

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

Condition / disease
Location
Status: Recruiting

Emerging Technologies and Teen Mental Health

This study will recruit teens who are experiencing subacute suicidal ideation to test the effect of a brief psychoeducational intervention focused on social media use wherein youth learn about active and prosocial use of social media platforms.

Participants needed: 200
Trial details
Age: 12-17Biological sex: AllType: InterventionalSponsor: Florida International UniversityUpdated: Apr 14, 2026Locations: 1
Eligibility criteria

Adolescents must (A) be between ages 12 and 17 years [+4]

Adolescents must not (A) have cognitive impairment or developmental delay which... [+1]

Status: Recruiting

intErnet-based iNterventions FOR Cardiac arrEst suRvivors

This randomized clinical trial will test whether an internet-based lifestyle intervention administered through a web app can foster Health Related Quality of Life in patients who survived an out-of-hospital cardiac arrest and suffer from these symptoms

Participants needed: 106
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Azienda Usl di BolognaUpdated: Mar 30, 2026Locations: 2
Eligibility criteria

Hospital discharge after out-of-hospital cardiac arrest with Cerebral Performanc... [+3]

Previous cognitive dysfunction [+2]

Status: Recruiting

Project HOPEFUL: A PN-RCT With Implementation Science

This PN-RCT replicates and evaluates an 8-week warm calling treatment (i.e. caring contacts) delivered to older adults receiving home and community-based services (HCBS; classified as "homebound") in 20-30 minute call "dosages", across 3 conditions, while adding in implementation science measures at multiple levels. Conditions include 2 treatment (i.e. treatment provided by helpers trained in a standardized and manualized Belongingness and Empathy training grounded in narrative reminiscence and the befriending literature (BE condition), and treatment provided by helpers trained in BE + a standardized, manualized, and evidence based suicide intervention training, the Aging Variant of LivingWorks ASIST (BE + ASIST condition), and 1 control (no treatment during the trial; opportunity to receive treatment after the 8 weeks). At the conclusion of treatment, acceptability, appropriateness, feasibility, useability, and sustainability of the program will be evaluated by interventionists, senior center leadership, and regional leadership.

Participants needed: 400
Trial details
Age: 55+Biological sex: AllType: InterventionalSponsor: University of FloridaUpdated: Mar 16, 2026Locations: 1
Eligibility criteria

Provision of verbal informed consent [+12]

Had a dementia diagnosis, or another form of cognitive impairment, and/or hearin... [+5]

Status: Recruiting

Psychological Correlates of Developmental Delays in Preschool Children

The goal of this observational study is to investigate perinatal, cognitive, linguistic and social-emotional correlates of developmental delays of preschool children. The study group consist of minimal 500 children between 3 and 6 years of age who will be examined by qualified diagnosticians. Participants will be evaluated with tasks related to the studied variables: cognitive functioning, linguistic skills and social-emotional functioning. Furthermore informations regarding social-emotional functioning of children, will be collected from parents. The main questions it aims to answer are: 1. Is there a relationship between perinatal factors and risk of occurrence of developmental delay disorder? 2. Is there a specific pattern of cognitive functioning in preschool children with indicated developmental delay disorder? 3. Is there a specific pattern of social-emotional functioning in preschool children with indicated developmental delay disorder? 4. Do gender and age moderates specific patterns of cognitive and socialemotional functioning in the studied groups? Researchers will compare the following groups of children between 3 and 6 years old: 1. With perinatal risks factors 2. With developmental delay disorder: 1. children with early intervention 2. children with delayed speech development 3. Control group

Participants needed: 500
Trial details
Age: 3-6Biological sex: AllType: ObservationalSponsor: Bartosz M. RadtkeUpdated: Feb 19, 2026Locations: 1
Eligibility criteria

Children aged 3 to 6 years at the time of assessment. [+4]

Age below 3 years or above 6 years. [+3]

Status: Recruiting

Hybrid Type 1 Randomized Pilot Trial of a Peer-led Family and Social Strengthening Group Intervention for Refugee Families

The proposed study draws on prior research to evaluate the feasibility, acceptability and explore preliminary effectiveness of Coffee and Family Education and Support, Version (CAFES2) using a pilot randomized type 1 hybrid effectiveness-implementation design. CAFES2 is a peer-led family and social strengthening multiple family group intervention that is designed to respond to multi-level needs of refugee families. Results of the trial will contribute to the emerging evidence base on family-based mental health interventions for refugee and newcomer communities. The trial will also generate new insights regarding implementation strategies needed to promote successful delivery of services by peer providers and the unique role of human-centered design practices for adaptation of mental health and psychosocial interventions.

Participants needed: 74
Trial details
Age: 12-55Biological sex: AllType: InterventionalSponsor: University of Illinois at ChicagoUpdated: Oct 1, 2025Locations: 1
Eligibility criteria

Country of origin: Iraq, Syria, Lebanon, Jordan, Palestine or Yemen [+4]

Not from one of the following Arabic-speaking countries in the Middle East: Iraq... [+4]

Status: Recruiting

Characteristics of Injury Claims by Chronic Pain Patients

Chronic pain is associated with injuries and disabilities. This prospective observational study explores the injury or disability claims made by chronic pain patients. It evaluates the socio-demographics of the patient population. It explores the impact of pain clinic services on the patients' injury rehabilitation, insurance claim outcome, and socioeconomic situation.

Participants needed: 1,000
Trial details
Age: 20-99Biological sex: AllType: ObservationalSponsor: Salem Anaesthesia Pain ClinicUpdated: Jan 27, 2025Locations: 1
Eligibility criteria

adult chronic pain patients [+1]

pediatric patients [+1]

Status: Recruiting

Pain Clinic Provides Public Health Safety

Chronic pain is associated with psychological disorders; which may affect a patient's socioeconomic, legal, domestic, and employment situations. This prospective observational study evaluates the impact of pain management on patients' health, social, economic, and employment status. It explores the impact of pain clinic services on patients' mental health, family health, public health, road safety, addiction situation, public safety, injury rehabilitation and employment situation.

Participants needed: 1,000
Trial details
Age: 20-99Biological sex: AllType: ObservationalSponsor: Salem Anaesthesia Pain ClinicUpdated: Jan 27, 2025Locations: 1
Eligibility criteria

adult chronic pain patients [+1]

pediatric patients [+1]

Status: Recruiting

The PRISM-Social Needs (PRISM-SN) Intervention for Adolescents and Young Adults With Cancer

The goal of this study is to establish feasibility, acceptability, and proof-of-concept of an psychosocial intervention adapted to address social health needs of adolescents and young adults (AYAs) newly diagnosed with cancer. The aims of this study are to: 1. Determine if the Promoting Resilience in Stress Management - Social Needs (PRISM-SN) adapted intervention is feasible and acceptable, defined via program uptake and retention and patient-reported feedback. 2. Explore whether PRISM-SN improves social outcomes at 12-week follow-up compared to usual care. Participants will be randomized to receive usual psychosocial care or the PRISM-SN program. Participants on both arms will complete patient-reported outcome surveys at enrollment and 12-weeks later. Researchers will compare participants who received the PRISM-SN program to those who received usual care to see if the program improves psychosocial outcomes.

Participants needed: 100
Trial details
Age: 12-25Biological sex: AllType: InterventionalSponsor: Seattle Children's HospitalUpdated: Jun 25, 2024Locations: 1
Eligibility criteria

Aged 12-25 years [+4]

Aged <12 or >25 years [+6]