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Nutool therapy in stress management

Effect of Nutool therapy in stress management. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/081303
Enrollment
10
Registered
2025-02-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: F430- Acute stress reaction Health Condition 2: F430- Acute stress reaction

Interventions

Intervention1: nil: nil Control Intervention1: not applicable: not applicable

Sponsors

Ajmal Khan tibbiya college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The patients for the study will be selected from the following criteria: 1. Diagnosed cases of stress. 2. Age between 20 and 45 years of age of both sexes. 3. Patients willing to give informed written consent.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1. Age below 20 and above 45 years of age. 2. Patients who refuse to sign the consent. 3. Patients with concurrent systemic illness. 4. Patients on any other medications. 5. Pregnant and lactating patients.

Design outcomes

Primary

MeasureTime frame
Changes in perceived stress scale (PSS) in every 2 weeks for 8 weeksTimepoint: Changes in perceived stress scale (PSS) in every 2 weeks for 8 weeks—

Secondary

MeasureTime frame
Improvement in the Objective parameters assessed clinically by PsychiatristTimepoint: After 3 weeks—

Countries

India

Contacts

Public ContactDr M Shoaib

Ajmal Khan tibbiya college

drmshoaib77@gmail.com9411491568

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026