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Clinical Trials/NCT05799677
NCT05799677CompletedNot Applicable

The Effect of Reflexology in Patients With Viral Bronchiolitis

Hillel Yaffe Medical Center1 site in 1 country30 target enrollmentStarted: January 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
Oxygen therapy period

Study Overview

Brief Summary

To test the influence of reflexology on bronchiolitis.

Detailed Description

Reflexology has been used in different respiratory tract infections on pulmonary function tests in patients with asthma, with some success. It has also been tested in newborns with respiratory distress syndrome, where it has decreased respiratory rate. Whole body massage was found to be helpful in newborns with opioid withdrawal syndrome. It has been shown to be a safe treatment and well tolerated even among very young infants.

Therefore, the investigators decided to evaluate effect of reflexology treatment in patients with viral bronchiolitis.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
— to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •All children admitted due to bronchiolitis

Exclusion Criteria

  • •Children whose parents refused participation

Arms & Interventions

Reflexology

Experimental

Additive treatment with reflexology

Intervention: Reflexology (Other)

Control

No Intervention

No treatment with reflexology

Outcomes

Primary Outcomes

Oxygen therapy period

Time Frame: 1-14 Days

Number of days of oxygen treatment

Hospitalization period

Time Frame: 1-14 days

The time from admission to discharge (days)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Erez Nadir, MD

Principal Investigator

Hillel Yaffe Medical Center

Study Sites (1)

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