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EL-SHIN Therapy for Depressive Symptoms

Enhancing the Efficacy of Depression and Low Mood Treatment: A Novel Adjunctive Approach

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06995807
Enrollment
80
Registered
2025-05-30
Start date
2025-06-01
Completion date
2027-05-31
Last updated
2025-12-01

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

Conditions

Depressive Disorder

Brief summary

This is a research aiming to find the effectiveness of an innovative therapy, EL-SHIN THERAPY, in ameliorating depressive symptoms.

Detailed description

This study evaluates the effectiveness of EL-SHIN® Therapy, a novel adjunctive intervention in alleviating depressive symptoms. There are three components in this therapy: 1. Lavender Therapy 2. GRATEFULNESS® Therapy 3. Fasting with exercise and light therapy The study includes two phases: a quantitative clinical trial and a qualitative focus group. Assessments will use DASS-21, MHQoL, and SQS scales with the intervention delivered in English over 3-4 weeks.

Interventions

OTHEREL-SHIN THERAPY

Participants will be randomly assigned to Group A and Group B. Group A : Attend a talk on Malaysia Tourism + current coping strategies. Group B : EL-SHIN® Therapy + current coping strategies. Duration of therapies: 2 weeks Assessments using (i) DASS-21 (ii) MHQoL (iii) SLEEP QUALITY SCALE (SQS) at baseline, after 1st week & 2nd weeks for both groups. Assessment will be done on end of 3rd week to see effect when EL-SHIN Therapy Stopped. Group B participants: Attend a workshop on administration of EL-SHIN® Therapy. Will reinitiate EL-SHIN Therapy on the 4th week and assess on the 8th day to see the effect.

Sponsors

Monash University Malaysia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Participants will be randomly assigned to either continue standard treatment with a control activity (Group A) or receive EL-SHIN® Therapy alongside their usual care (Group B).

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age: Above 18 yrs old * DASS-21 scores: Moderately Depressed (Score: 14-20), Moderately Anxious (Score: 10-14) & Moderately Stressed (Score: 19-25) * Non-Muslim (Due to legal restriction in Malaysia for this religion) * English literate * Believers in Creationism

Exclusion criteria

* Muslim (legal restrictions in Malaysia for this religion). * Non-English literate (research will be conducted in English only). * Individuals with any other medical conditions or on current medication To reduce potential complications or confounding factors).

Design outcomes

Primary

MeasureTime frameDescription
DASS-21 Scale3 to 4 weeksMeasuring severity of Depression, Anxiety and Stress Level. Higher score indicating more severity in experiencing these symptoms
Mental Health Quality of Life (MHQoL)3 to 4 weeksMeasuring quality of life of individuals. Higher score indicating better quality of life.
Sleep Quality Scale (SQS)3 to 4 weeksMeasuring Sleep Quality of Individuals with higher score denoting more acute sleep problem

Countries

Malaysia

Contacts

Primary ContactAI SHIN LIM, PHD
Ai.lim@monash.edu+60162303067
Backup ContactAI SHIN LIM

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026