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Pilot RCT Using Homeopathic Medicines in ASD

A Single-blind Randomized Placebo Controlled Pilot Study With Individualized Homeopathic Treatment in the Children With Autism Spectrum Disorder (ASD)

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07161804
Acronym
Pilot-RCT-ASD
Enrollment
54
Registered
2025-09-09
Start date
2016-12-31
Completion date
2025-01-13
Last updated
2025-11-18

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

Conditions

Autism Spectrum Disorder (ASD)

Keywords

ASD, RCT, HOMEOPATHY

Brief summary

This study looked at whether homeopathic treatment could help children with Autism Spectrum Disorder (ASD) when used alongside regular therapies like speech and occupational therapy. Over seven years, children between the ages of 3 and 12 were divided into two groups (through computer generated list). One group received individualized homeopathic medicines, and the other received a look-alike placebo (with no active ingredients). Meanwhile, both the groups continued with their regular therapies. Researchers used various tools and parent questionnaires to track the children's progress in areas like communication, behavior, social skills, daily functioning, toilet training and sensory skills.

Detailed description

Autism spectrum disorders (ASD) are lifetime neurodevelopmental disorders with challenges across functional domains. Despite availability of various treatment modalities and diagnostic tools, it's pathophysiology still remains poorly understood even through 8 decades of it's discovery. This pilot study compares psychometrics and parental reported outcome monitoring, behavioral and developmental outcomes, co-occurring breadth of concerns for children with ASD along with co-morbidities, with and without homeopathic treatment. Methodology: Initial screening was done using Autism Behavior Checklist (ABC). Utilizing a randomized-controlled design and parental informed consent, this study compared children aged 3 to 12 years, divided into an experimental group receiving individualized homeopathic treatment alongside occupational/speech therapies (HG), and a control group receiving only latter (CG) . The treatment group received homoeopathic medicines daily with frequency being once per day along with daily occupational / speech therapy sessions for 1 hour each. The control group received homoeopathic medicine look alike placebo daily with frequency being once per day along with daily occupational / speech therapy sessions for 1 hour each. Follow ups were done every 3 months and the data were combined and stored for each year separately for seven-years. The data was initially collected and then analyzed through standardized behavioral assessments \[Childhood Autism Rating Scale, CARS\] , speech-language assessments \[Social Responsiveness Scale, SRS\], parental-questionnaires for reporting emotional regulation, anxiety-related behaviors, co-morbidities \[Neuro Developmental Parent Report for Outcome Monitoring, ND-PROM\] and observational methods in both the groups. The treatment effectiveness was assessed using Autism Treatment Evaluation Checklist (ATEC).

Interventions

Thuja officinalis Vaccininum Causticum Argentum nitricum Tuberculinum Stramonium Staphysagria Arum triphyllum Bacillinum Cina Carcinocin Cuprum Metallicum Ambera grisea Calcarea carbonica Crocus sativus Hepar sulphur Hyoscymus Kali Bromatum Lac Vaccininum Medorrhinum Natrum phosphoricum Thyroidinum

BEHAVIORALTherapy

Occupational Therapy / Speech Therapy

DRUGPlacebo

Saccharum lactis

Sponsors

Holistic Homoeopathic Clinic and Research Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* A confirmed diagnosis of Autism Spectrum Disorder (ABC score ≥ 67) * Age range of 2 to 12 years

Exclusion criteria

* Children with other significant comorbid psychiatric conditions that could confound the results. \[eg. a brain injury; fragile X syndrome or other syndromes resulting from known genetic defects or inherited metabolic diseases; other diagnosed conditions involving impairments in social and communication abilities, such as intellectual disability without ASD, global developmental delay, language disorders and social communication disorder\] * Children with irregular follow ups. * Children with poor medical compliance.

Design outcomes

Primary

MeasureTime frameDescription
Childhood Autism Rating Scale (CARS)Baseline, Yearly (0 - 7 years)To measure various behavioral dimensions and adaptive functioning
Autism Treatment Evaluation Checklist (ATEC)Baseline, Yearly (0 - 7 years)To assess the efficacy of the treatment among both the arms.

Secondary

MeasureTime frameDescription
Social Responsiveness Scale (SRS)Baseline, Yearly (0 - 7 years)To measure social skills, communication abilities.
Neurodevelopmental Parent Report for Outcome Monitoring (ND PROM)Baseline, Yearly (0 - 7 years)To gather subjective reports on their children's behavior, social interactions, and overall well-being from the parents.

Countries

India

Outcome results

None listed

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