Università degli Studi di Padova
Padova, 35131, Italy
Location status: Recruiting
NCT Number: NCT07147712
This study evaluates the impact of a psychological group intervention aimed at promoting well-being and social connectedness among university students. The intervention is part of the UNIST-HEALTH (PRO-BEN) initiative and targets students enrolled at the University of Padua. Participants will be randomly assigned to either an intervention group or a waitlist control group. The intervention consists of six weekly group sessions focused on psychoeducation and experiential activities designed to enhance the quality of social relationships, reduce loneliness, and improve psychological well-being. Assessments will be conducted at baseline, post-intervention, and at a four-week follow-up.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Padova, 35131, Italy
Location status: Recruiting
University students are a population at heightened risk for psychological distress, with increasing levels of loneliness, anxiety, and depression reported globally. The university period represents a developmental transition characterized by academic, social, and emotional challenges.
Extensive research has shown that strong social relationships are critical to psychological well-being. High levels of social connectedness are associated with lower rates of anxiety and depression, and promote greater life satisfaction, emotional resilience, and academic adjustment. In contrast, loneliness and perceived social isolation are predictors of psychological distress and negative health outcomes.
To address these issues, the aim of this study is to evaluate the impact of a brief psychological group intervention designed to promote well-being and enhance the quality of social relationships among university students. The intervention is developed within the framework of the UNIST-HEALTH (PRO-BEN) project.
Assessment Phase The study begins with an initial screening phase. Participants are invited to attend a brief individual interview with a trained psychologist to assess their psychological health status, motivation to participate, and expectations regarding the intervention.
Following the interview, participants complete a baseline questionnaire collecting demographic information (e.g. age, gender, course of study, country of origin, type of housing - 10 questions) and measures from self-report instruments, including:
Participants complete the same set of questionnaires at three time points:
The study aims:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
6-session psychological group intervention, delivered once per week over six weeks. The intervention is designed to promote well-being and improve the quality of social relationships. It includes psychoeducational content, experiential exercises, and guided group discussions focused on emotional expression, social connection, and mutual support. A follow-up session will be offered after 4 weeks. Sessions will be led by trained psychologists and conducted in a university setting.
Time frame: baseline, 6-weeks, 4-weeks follow-up
Psychological Well-Being Scale (PWS; min=18, max=108; higher scores indicate greater wellbeing)
Time frame: baseline, 6-weeks, 4-weeks follow-up
UCLA Loneliness Scale - 3-item version (min=3, max=9; higher scores indicate higher levels of loneliness)
Time frame: 6-weeks, 4-weeks follow-up
Participants' attendance rates to the sessions
Time frame: 6-weeks
Participants' rates to the satisfaction questionnaire, developed ad hoc for the present study (min=8, max= 56; higher scores indicate higher satisfaction)
Time frame: baseline, 6-weeks, 4-weeks follow-up
General Anxiety Disorder-7 (GAD-7). Higher scores indicate greater anxiety severity (min=0, max=21)
Time frame: baseline, 6-weeks, 4-weeks follow-up
Patient Health Questionnaire-9 (PHQ-9). A higher score means more severe symptoms (min=0, max=27)
Contact information is provided by the study sponsor or research team.
University of Padova
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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