Long Covid (Individuals with Ongoing COVID-19 Symptoms) Ongoing Effects

NCT ID: NCT06528145

Last Updated: 2025-02-12

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

Total Enrollment

70 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-09-25

Study Completion Date

2023-02-20

Brief Summary

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Persistent Covid-19 symptoms, known as long Covid, can impact healthcare provision. This study aimed to assess how symptoms persisting six months after Covid-19 affect quality of life and functional capacity.

Detailed Description

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Conditions

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COVID-19 Infection

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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S-

Individuals who have not had symptoms for 6-18 months after Covid infection

Evalation

Intervention Type OTHER

Post Covid Functional Scale (PCFS) was used to assess the functional status of the participants; Short Form- 36 (SF-36) questionnaire was used to assess quality of life; 30 s sit-to-stand test (30s-STS) and 6 min walk test (6 MWT) were used to assess functional capacity.

S+

Individuals with ongoing symptoms 6-18 months after Covid infection

Evalation

Intervention Type OTHER

Post Covid Functional Scale (PCFS) was used to assess the functional status of the participants; Short Form- 36 (SF-36) questionnaire was used to assess quality of life; 30 s sit-to-stand test (30s-STS) and 6 min walk test (6 MWT) were used to assess functional capacity.

Interventions

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Evalation

Post Covid Functional Scale (PCFS) was used to assess the functional status of the participants; Short Form- 36 (SF-36) questionnaire was used to assess quality of life; 30 s sit-to-stand test (30s-STS) and 6 min walk test (6 MWT) were used to assess functional capacity.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* The study included individuals who had Covid-19 disease at least 6-18 months ago, who agreed to participate, and who were diagnosed with Covid-19 by a health institu-tion during the disease period.

Exclusion Criteria

* Individuals who were not between the ages of 18-65, who had cognitive and commu-nicative impairments, and who had orthopedic and neurological limitations that would prevent them from performing physical activity were excluded from the study.
Minimum Eligible Age

18 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Suleyman Demirel University

OTHER

Sponsor Role collaborator

Pamukkale University

OTHER

Sponsor Role collaborator

Ziya Yildiz

OTHER

Sponsor Role lead

Responsible Party

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Ziya Yildiz

Dr. PhD (physiotherapy and rehabilitation)

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Süleyman Demirel Univesity

Isparta, Isparta, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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SülDemirelUni_YildizA_002

Identifier Type: -

Identifier Source: org_study_id

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