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Full Wet Sheet Pack Therapy on Sleep, Stress, Thinking Ability, and Body Functions in Adults with Insomnia

Effect of 4 Weeks Full Wet Sheet Pack Therapy on Autonomic variables,Perceived Stress,Cognitive Function and Sleep Quality in Adults with Insomnia-A Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/07/113348
Enrollment
90
Registered
2026-07-03
Start date
Unknown
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

Health Condition 1: F510- Insomnia not due to a substance orknown physiological condition

Interventions

Intervention1: Full Wet Sheet Pack Therapy: Participants randomized to the intervention group will receive Full Wet Sheet Pack Therapy in addition to standard care. The therapy will be administered th

Sponsors

RITHIK NARAYANAN
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Presence of insomnia symptoms for at least one month, including difficulty initiating sleep, difficulty maintaining sleep, early morning awakening, or dissatisfaction with sleep Presence of daytime impairment related to insomnia, such as fatigue, reduced work performance, impaired social functioning, or difficulty performing routine daily activities Ability to understand the study procedures and provide written informed consent.

Exclusion criteria

Exclusion criteria: Participants with serious or worsening health conditions, including illnesses like cancer, severe ongoing pain, or disorders affecting the brain such as dementia, will be excluded Individuals having unstable psychological conditions, including psychotic disorders, bipolar disorder, repeated episodes of depression, or any untreated mental health problem, will not be included in the study People who are engaged in night shift work and are unable to modify or stop this schedule during the study period will be excluded Individuals with present alcohol or substance abuse problem

Design outcomes

Primary

MeasureTime frame
Pittsburgh Sleep Quality Index Serum CortisolTimepoint: Baseline- Day 0 Post data- after 4 weeks of intervention

Secondary

MeasureTime frame
Heart Rate Variability Blood Pressure Perceived Stress Scale Montreal Cognitive Assessment Timepoint: Baseline- Day 0 Post data- after 4 weeks of intervention

Countries

India

Contacts

Public ContactDR NAIR DHIREN AJIT

Maharishi Aurobindo Subharti College And Hospital of Naturopathy And Yogic Sciences

danny.a.nair@gmail.com7899143619

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026