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Effect of Probiotic Nata Jelly from Pineapple Juice on Depressive, Anxiety and Stress Symptoms

Effect of Probiotic Nata Jelly from Pineapple Juice on Depressive, Anxiety and Stress Symptoms

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20221123005
Enrollment
70
Registered
2022-11-23
Start date
2022-03-01
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

Healthy condition Probiotic Nata Jelly Pineapple Depression Anxiety Stress

Interventions

Subjects are received the placebo product which has the same color and smell looks like Probiotic Nata Jelly from Pineapple Juice.,Subjects are received Probiotic Nata Jelly from Pineapple Juice.
Placebo,Probiotic Nata Jelly from Pineapple Juice

Sponsors

National Research Council of Thailand (NRCT)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Healthy volunteers aged between 30-65 years old who live in Northeastern of Thailand. 2. Volunteers don't have menopause syndromes. 3. All volunteers don't have serious physical illnesses such as diabetes, high blood pressure, heart disease, liver disease, kidney disease, lung disease or allergies, and mental disorders. 4. All volunteers don't get medicine or hormone or other medicines that affect the nervous system and bone during the trial and within three months before the start of the test. 5. All volunteers don't smoke more than 10 pieces per day 6. All volunteers don't have an alcohol addiction 7. On the study day, all volunteers felt well and refrain from drinking tea, coffee, or alcohol at least 12 hours.

Exclusion criteria

Exclusion criteria: 1. Volunteers who have been diagnosed with one of the following; cardiovascular diseases, respiratory diseases, neurological diseases, psychiatric disorders, head injury, diabetes mellitus, liver disease, cancer, autoimmune disease, hematological disorder, and gout or high uric acid. 2. Volunteers who were exposed to pesticides during one week before the test. 3. Volunteers who have been Hysterectomy and/or Oophorectomy. 4. Volunteers who require supplements or any drug that effect on the nervous system by order of the doctor during the trial. 5. Volunteers who participate in other projects.

Design outcomes

Primary

MeasureTime frame
Depressive, Anxiety and Stress Symptoms 8 weeks Depression Anxiety Stress Scale 21 Thai (DASS-21 Thai)

Secondary

MeasureTime frame
Positive mood evaluation 8 weeks MOSAIC questionnaire,Sleep quality 8 weeks Pittsburgh Sleep Quality Index - Thai (PSQI- Thai),The changes of oxidative stress status 8 weeks Laboratory,The changes of 5-hydroxytryptamine (5-HT) and melatonin 8 weeks ELISA Kit,Serum cortisol 8 weeks Laboratory,Working memory test 8 weeks Computerized cognitive batteries test ,The changes of hematological and clinical chemistry parameters 8 weeks Laboratory

Countries

Thailand

Contacts

Public ContactPongsatorn Paholpak

Faculty of Medicine, Khon Kaen University

ppaholpak@kku.ac.th0894221147

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026