Community-based Individualized Homeopathic Rehabilitation in Post COVID-19 Patients

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

69 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-08-06

Study Completion Date

2023-01-12

Brief Summary

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A growing number of studies identify a spectrum of persistent symptoms experienced by COVID-19 patients for months after recovery. Symptoms include cough, fatigue, dyspnea, pain, and brain fog (cognitive impairment, including confusion and memory loss), which have a negative impact on daily activities. Homoeopathic practitioners from around the world have documented a number of successful cases of Post COVID treatment. Even though evidence from practice-based research is limited, the purpose of the current study was to evaluate the effect of individualized homoeopathy treatment on post-COVID syndrome.

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Detailed Description

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Conditions

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Post-COVID Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Homeopathy Group

Individualized Homeopathy Treatment provided by homeopathic physicians

Group Type EXPERIMENTAL

Homeopathy

Intervention Type OTHER

Individualized homoeopathic medicines on impregnated lactose pellets was prescribed based on totality of physical, emotional, and mental symptoms.

Standard Group

Usual care provided by primary care physicians were followed by patients in the standard group

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Homeopathy

Individualized homoeopathic medicines on impregnated lactose pellets was prescribed based on totality of physical, emotional, and mental symptoms.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Confirmed COVID-19 history
* Persistent respiratory symptoms for more than three months after COVID-19
* Able to provide informed consent

Exclusion Criteria

* Presence of respiratory issues without COVID-19 diagnosis
* On complementary and Alternative Treatment
* Symptoms of infection
* Pregnancy or Breastfeeding
* Cognitive impairment

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No