ClinicalTrials.gg
Not yet recruitingNCT07574021Updated May 7, 2026

The Experience of Short Video Addiction Among College Students

An observational study in Behavior, Addictive and College Student, sponsored by Sun Yat-sen University. Not yet recruiting at 1 site in China. Open to participants aged 18 Years to 30 Years. Per ClinicalTrials.gov, last updated 2026-05-07.

Sponsored by Sun Yat-sen University · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2026, 5 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
30
Ages
18 Years to 30 Years
Sex
All
01

Study summary

This qualitative study aims to explore the experience of short-video addiction among college students using a directed content analysis approach grounded in the integrated framework of the Stimulus-Organism-Response (S-O-R) theory and the Temporal Self-Regulation Theory (TST).

Read the detailed description

Short-form videos have become one of the most popular ways for people to entertain and relax. However, the intense interest in short-form videos has given rise to short-video addiction, which poses risks to both physical and mental health of individuals. As undergraduates constitute a key user group of short-form videos, the associated adverse outcomes of short-form video addiction-including poor sleep, physical discomfort, academic procrastination, anxiety, and impaired self-regulation-call for increased attention.Understanding its underlying mechanisms is therefore critical, yet existing quantitative studies lack contextual depth, and qualitative research remains sparse and theoretically fragmented.To address this gap, this qualitative study will use directed content analysis grounded in an integrated Stimulus-Organism-Response (S-O-R) and Temporal Self-Regulation Theory (TST) framework. Eligible full-time college students will complete semi-structured interviews exploring triggering stimuli, emotional/cognitive responses, behavioral consequences, time perception, future self-connection, and self-regulatory failures. The study will produce a theory-driven, empirically grounded model of short video addiction formation, informing targeted prevention and intervention strategies for this high-risk population.

02

Conditions studied

  • Behavior, Addictive
  • College Student

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Keywords

  • Short video addiction
  • college student
  • Qualitative Research
  • Stimulus-Organism-Response Theory
  • Temporal Self-Regulation Theory
03

In context

Behavior, Addictive

521 studies on the registry are indexed under Behavior, Addictive; 124 are open to participants now.

This study's planned enrollment of 30 is below the median of 158 across 106 observational studies indexed under Behavior, Addictive.

Browse Behavior, Addictive studies →

Lead sponsor

Sun Yat-sen University is the lead sponsor of 1,690 studies on the registry; 619 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

The study population will consist of full-time college students (including associate degree, bachelor's degree, and graduate students) recruited from universities in China. Participants will be purposively selected based on their scores on the College Student Short Video Addiction Scale. Those who answer "yes" to 4 or more diagnostic items on the scale will be included, indicating a pattern of problematic short video use. Individuals with severe mental disorders or major cognitive impairment participation will be excluded.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Full-time college students (including associate degree, bachelor's degree, and graduate students)
  • Answer "yes" to 4 or more diagnostic items on the College Student Short Video Addiction Scale
  • Willing to participate voluntarily and provide written

Exclusion criteria

Exclusion Criteria:

  • Those with severe mental or cognitive impairments who are unable to participate in the interview.
  • Refusal to participate in the study
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
30 participants (estimated)
Patient registry
No

Groups and cohorts

  • College students with short video addiction

    Full-time college students (associate, bachelor, or graduate) who meet the screening criterion of 4 or more affirmative responses on the College Student Short Video Addiction Scale.

    Other: Semistructured interview

Interventions

  • OtherSemistructured interview

    A qualitative design using directed content analysis will be employed. Participants will be full-time college students who meet the screening criteria based on the College Student Short Video Addiction Scale. A semi-structured interview approach will be adopted to collect data on aspects such as the history of college students' use of short videos, triggering situations, emotional and cognitive experiences, self-regulation strategies, and perceived impacts.

06

What researchers measure

Primary outcomes

  1. Qualitative Experience of Short Video Addiction

    Thematic patterns of short video addiction based on the integrated S-O-R and TST framework, including triggering stimuli, emotional/cognitive experiences, behavioral responses, time perception distortion, future self-connection, and self-regulatory failure.

    Time frame: At the time of interview

07

Study locations

1 site
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for May 2026; primary completion for Jun 2026, 1 month later.

Of 46 non-industry observational studies under Behavior, Addictive, half reached primary completion within 40 months of starting (the median), counting those still running; a quarter within 20 and three quarters within 111. This study's planned 1 month is below that.

Counting every sponsor, half of 49 studies reached it within 40 months; a quarter within 20 and three quarters within 73.

How these figures are worked out, and which studies are left out of them.

Registered
May 1, 2026
First posted
May 7, 2026
StartEst.
May 1, 2026
Primary completionEst.
Jun 1, 2026
CompletionEst.
Jun 1, 2026
Last update
May 7, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07574021
Responsible party
Wei XIA, PhD (Associate Professor, Sun Yat-sen University) — Principal investigator
First posted
May 7, 2026
Start date
May 1, 2026 (estimated)
Primary completion
Jun 1, 2026 (estimated)
Completion
Jun 1, 2026 (estimated)
Last update
May 7, 2026

Study contacts

Wei Xia
Contact
xiaw23@mail.sysu.edu.cn
18823359471
Yuke Zhu
Contact
ZhuKke041@163.com
18001559380
Wei Xia
principal investigator · Sun Yat-sen University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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