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Evaluation of Efficacy of Lycium Barbarum Polysaccharide in People With Subthreshold Depression

Evaluation of Efficacy of Lycium Barbarum Polysaccharide in People With Subthreshold Depression: a Randomized, Placebo-controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04032795
Enrollment
172
Registered
2019-07-25
Start date
2019-05-15
Completion date
2021-12-30
Last updated
2021-11-19

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

Conditions

Anxious Symptoms, Depressive Symptoms, Subthreshold Depression

Keywords

Major Depressive Disorder, Lycium barbarum polysaccharide, depressive symptoms, anxious symptoms

Brief summary

Lycium barbarum, a traditional Chinese herbal medicine, is a commonly used herb in the traditional Chinese pharmacopoeia . Its main active ingredient, lycium barbarum polysaccharide (LBP), is reported to have neuroprotective effects. Animal studies suggested that LBP has neuroprotective effect on optic ganglion cells. In animal models of depression, LBP can improve depressive symptom by improving synaptic plasticity. However, its clinical effect remains to be studied. We will conduct a 6-week double-blind, randomized, placebo-con-trolled trial in people with subthreshold depression.The purpose of this clinical trial is to investigate the efficacy of LBP in people with subthreshold depression.

Interventions

Experimental group takes Lycium barbarum polysaccharide (LBP) tablet (300mg/day)for 6 weeks

DIETARY_SUPPLEMENTPlacebo

Placebo-controlled group take he placebo capsules that are identical in shape, color, and taste to LBP tablet.

Sponsors

Fifth Affiliated Hospital of Guangzhou Medical University
CollaboratorOTHER
Guangzhou Psychiatric Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

1. 15-25 scores in the Beck Depression Rating Scale (BDI- II) 2. There is no contraindication of taking LBP.

Exclusion criteria

1. Current treatment for a mental health problem from a mental health professional 2. Current and lifetime history of psychiatric disorders (e.g major depressive disorder, as ascertained by CIDI 3. Systemic disease requiring regular medication. 4. There are suicidal ideation, suicidal attempt, suicide behavior and attempted suicide. 5. Dislike of or allergy to goji berry 6. Hormone or Endocrine therapeutic drugs are being taken. 7. Long-term use of lycium chinensis in recent three months

Design outcomes

Primary

MeasureTime frameDescription
Mean changes from baseline in the 21-item Hamilton Depression Rating Scale (24-HAMD)6 weeksThe 24-item HAM-D scale is widely used to assess the severity of depression.The scale is a 21-item assessment used to measure depression severity. Items were rated on a scale from 0 (symptoms not present) to a maximum of 2 to 4 (symptom extremely severe) for a total score ranging from 0 (not at all depressed) to 64 (severely depressed).

Secondary

MeasureTime frameDescription
Changes in The Screen for Child Anxiety Related Disorders (SCARED)4 and 6 weeksThe SCARED is a child and parent self-report instrument used to screen for childhood anxiety disorders including general anxiety disorder, separation anxiety disorder, panic disorder, and social phobia.
Changes in sleep quality6 weeksChanges in Pittsburgh Sleep Quality Index (PSQI)
Depression severity as measured by BDI2 and Kessler Scale (K10)6 weeksThe Kessler psychological distress scale (K10) is a widely used, simple self-report measure of psychological distress which can be used to identify those in need of further assessment for anxiety and depression.
Mean change from baseline in the Beck Depression Inventory-II (BDI-2)total scores6 weekThe BDI-II is a 21-item self-report measure of depressive symptom.Remission was defined as equal or less than 8 scores on BDI-2.

Other

MeasureTime frameDescription
Treatment-emergent symptom side effect (TESS) scale.4 and 6 weeksSide effect was evaluated by treatment-emergent symptom side effect (TESS) scale.

Countries

China

Contacts

Primary ContactKangguang Lin, MD
linkangguang@163.com8613560360144
Backup ContactXuan Mo, MD
mx7628@126.com8615622326389

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026