Clinical trial Recruiting at 2 sites Interventional Ages 18 to 30

Group-based IMPROVE Therapy for Problematic Internet Use in University Students

Official title: Effectiveness and Psychological Mechanisms of Group-based IMPROVE Therapy for Problematic Internet Use in University Students: A Single-blind Randomized Controlled Trial

Run by Sir Run Run Shaw Hospital · NCT07434778 · Data updated 2026-11-12

This study tests an 8-week group therapy program called IMPROVE to see if it can reduce problematic internet use in university students compared with an enhanced waitlist control.

Quick facts

Study typeInterventional
Ages18 Years to 30 Years
SexAll
Enrollment600 (estimated)
SponsorSir Run Run Shaw Hospital
Academic / other
Locations2 sites (Hangzhou, Zhejiang and 1 other locations)
StatusRecruiting
StartedMarch 17, 2026
Main results expectedJune 2027
Study endsJune 2028
Registry record updatedAugust 5, 2026
Trial IDNCT07434778 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

University students aged 18–30 with an IAT score of 50 or higher and access to a smartphone, who have not recently engaged in PIU-focused psychotherapy.

Probably not a fit

Individuals with recent psychotherapy for PIU, current severe physical/neurological conditions, or diagnosed psychiatric disorders may derive less benefit or be excluded.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized, single-blind trial will enroll 600 university students with moderate to severe problematic internet use and assign them to either the IMPROVE group therapy or an enhanced waitlist control. IMPROVE is a manualized, multimodal program combining cognitive-behavioral techniques, motivational elements, mindfulness, and social exercise, delivered in group sessions. The trial will measure changes in PIU severity using the Internet Addiction Test (IAT) from baseline to 8 weeks, with aims to evaluate efficacy, durability, and potential mechanisms of change. The study also includes digital psychoeducation newsletters and digital components to support accessibility and engagement. Participants must own a smartphone or similar device and meet eligibility criteria related to age, disease severity, and absence of recent psychotherapy or major psychiatric conditions.

Why it matters

Potential benefit: If effective, IMPROVE could offer a structured, scalable approach to reduce PIU symptoms and improve functioning among university students.

How similar studies have gone: Prior work on multimodal, group-based approaches shows promise but robust, large-scale trials in this space are still emerging.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. be university students aged between 18 and 30 years;
2. report subjective suffering regarding their own internet use and score 50 or above on the Internet Addiction Test (IAT), indicating at least a moderate level of PIU;
3. own a personal smartphone or other electronic communication device to ensure accessibility to digital intervention components;
4. provide written informed consent prior to enrollment.

Exclusion Criteria:

1. a self-reported history of substance use (excluding tobacco and alcohol) within the past 12 months;
2. current or previous participation in any form of psychotherapy for PIU;
3. the presence of severe physical or neurological conditions (e.g., organic brain diseases, history of traumatic brain injury, or coma);
4. a self-reported history of diagnosed psychiatric disorders (e.g., schizophrenia, bipolar disorder).

Where it's running

  • Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
    Hangzhou, Zhejiang, China
    Recruiting
  • Zhejiang University
    Hangzhou, Zhejiang, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.