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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.
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:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Experimental - Psychological Group Intervention | Experimental | Intervention Group (receives the program immediately) |
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| Control group - waitlist | No Intervention | 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. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Psychological Group Intervention | Behavioral | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| Between group differences (experimental vs control group) in wellbeing levels | Psychological Well-Being Scale (PWS; min=18, max=108; higher scores indicate greater wellbeing) | baseline, 6-weeks, 4-weeks follow-up |
| Between group differences (experimental vs control group) in loneliness levels | UCLA Loneliness Scale - 3-item version (min=3, max=9; higher scores indicate higher levels of loneliness) | baseline, 6-weeks, 4-weeks follow-up |
| Adherence to the intervention | Participants' attendance rates to the sessions | 6-weeks, 4-weeks follow-up |
| Acceptability of the intervention | Participants' rates to the satisfaction questionnaire, developed ad hoc for the present study (min=8, max= 56; higher scores indicate higher satisfaction) | 6-weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Between group differences (experimental vs control group) in symptoms of anxiety | General Anxiety Disorder-7 (GAD-7). Higher scores indicate greater anxiety severity (min=0, max=21) | baseline, 6-weeks, 4-weeks follow-up |
| Between group differences (experimental vs control group) in symptoms of depression |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sabrina Cipolletta, PhD | Contact | +39 049 827 7423 | sabrina.cipolletta@unipd.it |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Università degli Studi di Padova | Recruiting | Padova | Padova | 35131 | Italy |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 39664633 | Background | Cipolletta S, Tedoldi I, Tomaino SCM. A blended group intervention to promote social connectedness and wellbeing among international university students: an exploratory study. Front Psychol. 2024 Nov 27;15:1497544. doi: 10.3389/fpsyg.2024.1497544. eCollection 2024. |
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A plan will be established by the research team for data sharing following publication of the first manuscript
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| ID | Term |
|---|---|
| D000092862 | Psychological Well-Being |
| ID | Term |
|---|---|
| D010549 | Personal Satisfaction |
| D001519 | Behavior |
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This study will use a randomized controlled design to test the impact of a brief psychological group intervention on university students' psychological well-being and social connectedness. Participants will be randomly assigned to either the intervention group (immediate participation in the 6-session program) or the control group (waitlist, intervention after follow-up).
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Patient Health Questionnaire-9 (PHQ-9). A higher score means more severe symptoms (min=0, max=27) |
| baseline, 6-weeks, 4-weeks follow-up |