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Observational Study on the Clinical Efficacy of Scraping Therapy in Intervening Subclinical Depression Among University Students

Observational Study on the Clinical Efficacy of Scraping Therapy in Intervening Subclinical Depression Among University Students

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001721
Enrollment
Unknown
Registered
2026-07-13
Start date
2026-08-15
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

subthreshold depression

Interventions

Group A (Gua Sha group):gua sha
Control Group:Health Education

Sponsors

Nanjing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: (1) Meets the diagnostic criteria for subthreshold depression according to Western medical standards; (2) College students aged =18 years, currently enrolled, with no restriction on gender; (3) Self-Rating Depression Scale (SDS) score =16 points; (4) Hamilton Depression Rating Scale (HAMD-17) score: 7 = HAMD < 17; (5) Mentally alert and willing to sign the informed consent form to cooperate with the researchers in this study.

Exclusion criteria

Exclusion criteria: (1) Clinically diagnosed individuals with depression, a history of mental illness, or organic mental disorders; (2) Individuals currently receiving antidepressant treatment or who have participated in other clinical trials within the past 3 months; (3) Individuals with severe liver or kidney dysfunction, heart failure, or severe arrhythmia; (4) Pregnant, breastfeeding, or menstruating women; (5) Individuals with a history of alcohol abuse, misuse of psychiatric medications, or substance dependence; (6) Individuals with strong suicidal ideation or behaviors; (7) Individuals with contraindications for gua sha, such as skin damage on the back or coagulation disorders; (8) Participants who are students of the researchers. Any individual meeting any one of the above exclusion criteria will not be included in this study.

Design outcomes

Primary

MeasureTime frame
Hamilton-17 Item Depression Scale;

Secondary

MeasureTime frame
Depression Self-Rating Scale (DSRS) used in surveys;Pittsburgh Sleep Quality Index (PSQI);Interaction Anxiety Scale (IAS);Attention Control Scale(ACS);

Countries

China

Contacts

Public ContactXu Guihua

Nanjing University of Chinese Medicine

xgh_88@126.com13952049095

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Aug 10, 2026