Study on an anxiety treatment protocol

Effect of V-CALM protocol in patients with anxiety disorders A Pretest-Posttest design. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/087627

Enrollment

Registered

2025-05-26

Start date

Unknown

Completion date

Unknown

Last updated

2025-06-24

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

Conditions

Health Condition 1: F40-F48- Anxiety, dissociative, stress-related, somatoform and other nonpsychotic mental disorders

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosed case of mild-moderate anxiety disorders (Ham -A 18-24) as per Hamilton anxiety rating scale.

Exclusion criteria

Exclusion criteria: Those under allopathic medication for generalised anxiety disorders. Those having other comorbid psychiatric conditions. Substance abuse, pregnancy and lactating mothers. Those having significant medical conditions that may interfere with the practice of the protocol

Design outcomes

Primary

Measure	Time frame
Hamilton Anxiety Rating Scale Quality of life assessment using Q-LES-Q-SF scale Insomnia severity indexTimepoint: 0th day, after the last day of medication and the 70th day of the follow up follow-up period	—

Secondary

Measure	Time frame
not applicableTimepoint: not applicable	—

Countries

India

Contacts

Public ContactDr Dileep K S

Vaidyaratnam Ayurveda Foundation

adithyaksreedhar@gmail.com9447303675

Outcome results