Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07147712

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

Led by University of Padova · Updated on 2025-08-29

50

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

AI-Summary

What this Trial Is 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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Università degli Studi di Padova

Padova, Padova, Italy, 35131

Actively Recruiting

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Research Team

S

Sabrina Cipolletta, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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