Interventions to Promote Well-being and Social Relationships Among University Students

University of Padova

Status: Enrolling

Conditions: Psychological Well Being; Loneliness; Social Relationship

Treatments: Behavioral: Psychological Group Intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT07147712

1232-b

Details and patient eligibility

About

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.

Full description

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:

• Questions regarding health status and social life (e.g. social and sports activities practiced) - 11 questions.
• UCLA Loneliness Scale - 3-item version: 3 items to measure subjective feelings of loneliness and social isolation.
• Psychological Well-Being Scale: 18 items to measure psychological well-being.
• General Anxiety Disorder-7: 7 questions about the perception of anxious symptoms in the last two weeks.
• Patient Health Questionnaire-9: 9 questions about the frequency with which, in the last two weeks, different problems attributable to depressive symptoms have been faced.
• Work and Social Adjustment Scale: 5 questions about functioning in social and work life.
• Multidimensional Scale of Perceived Social Support: 12 questions to measure perceived support, in particular from friends, family and partners.
• Sense of community: brief scale developed ad hoc to evaluate perception of belongingness to different groups

Participants complete the same set of questionnaires at three time points:

• Baseline (pre-intervention)
• Post-intervention (after 6 weeks)
• Follow-up (4 weeks after the final session) Intervention Phase Eligible participants are randomly assigned to either the intervention group or the control group (waitlist). The intervention group will immediately take part in a 6-session group-based program (one session per week, for six consecutive weeks), while the control group will receive the same intervention only after the follow-up period has been completed. Sessions will include psychoeducational modules, experiential exercises, and guided group discussions.

The study aims:

• to assess the feasibility and acceptability of a 6-weeks intervention to promote psychological and general well-being on university students
• to assess the impact of the intervention compared to a control group who did not receive it

Enrollment: 50 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• University students regularly enrolled at the University of Padua
• Aged 18 years or older
• Able to understand and complete the questionnaires in Italian or English
• Residing in Padova or its province during the study period
• Providing informed consent for participation

Exclusion criteria

• Presence of severe psychological conditions requiring immediate or specialized clinical care, as identified during the initial screening interview
• Inability or unavailability to attend group sessions for the full 6-week duration

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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50 participants in 2 patient groups

Experimental - Psychological Group Intervention

Experimental group

Description:

Intervention Group (receives the program immediately)

Treatment:

Behavioral: Psychological Group Intervention

Control group - waitlist

No Intervention group

Description:

Participants in the waitlist control group will not take part in the intervention during the initial phase of the study. They will complete all assessments at the same time points as the experimental group (pre, post, and follow-up) and will be offered the same 6-session intervention after the follow-up data collection is complete.