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Behavioral Intervention

RESToRE for Long COVID Syndrome (RESToRE Trial)

N/A

Recruiting

Led By Anna Norweg, PhD

Research Sponsored by Columbia University

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 10 weeks

Awards & highlights

RESToRE Trial Summary

This trial will investigate if aerobic/breathing exercises can help people with long COVID. Participants will do a tailored 6-week home exercise program supervised by therapists.

Who is the study for?

This trial is for individuals experiencing long COVID, specifically those with post-COVID syndrome or exercise intolerance. Participants should be able to follow a home exercise program for 6 weeks and commit to sessions 5-6 days per week.Check my eligibility

What is being tested?

The study is testing if rehabilitation exercises can aid recovery from long COVID. It compares two types of exercises: aerobic rehabilitation and light stretching/breathing exercises, both supervised by therapists.See study design

What are the potential side effects?

Potential side effects are not explicitly listed but may include typical reactions to new exercise routines such as muscle soreness, fatigue, or shortness of breath within the limits of sub-symptom threshold activity.

RESToRE Trial Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 10 weeks

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~10 weeks

This trial's timeline: 3 weeks for screening, Varies for treatment, and 10 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Number of participants who adhered to session attendance

Number of participants who completed

Number of participants who enrolled

Secondary outcome measures

EuroQol: Education Quotient-5D Visual Analogue Scale score

General Symptom Questionnaire (SGQ-30) score

Global Change Assessment (GCA) score

+5 more

RESToRE Trial Design

2Treatment groups

Experimental Treatment

Active Control

Group I: RESToREExperimental Treatment1 Intervention

Participants will receive RESToRE, an interdisciplinary, hybrid 8- week intervention.

Group II: Light Stretching ExerciseActive Control1 Intervention

The control group will receive 8-week, attention-matched, stretching and breathing exercises, supervised by a rehabilitation clinician.

Do I qualify?Apply below to find out

Find a Location

Who is running the clinical trial?

New York UniversityOTHER

226 Previous Clinical Trials

314,235 Total Patients Enrolled

Columbia UniversityLead Sponsor

1,431 Previous Clinical Trials

2,460,811 Total Patients Enrolled

Anna Norweg, PhDPrincipal InvestigatorColumbia University

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the magnitude of people enrolled in this experiment?

"Affirmative. Clinicaltrials.gov indicates that this trial is still open for recruitment, having been initially posted on October 1st 2023 and last updated on December 14th 2023. Currently, the study needs to find 20 volunteers at a single location."

Answered by AI

Is the study open to those of advanced age?

"To qualify for this medical trial, one must be aged 18 to 70. Additionally, there are 11 trials specifically designed for minors and 127 clinical studies targeting senior citizens."

Answered by AI

Is this research project recruiting participants at present?

"Affirmative, the information on clinicaltrials.gov demonstrates that this medical trial is actively enrolling participants. It was first posted on October 1st 2023 and has since been updated on December 14th with a goal of recruiting 20 patients from one site."

Answered by AI

Is it possible for me to become part of this experiment?

"To become eligible for this trial, applicants must be afflicted with long covid syndrome and within the age range of 18-70. Approximately 20 patients are needed to participate in the program."

Answered by AI

What are the primary objectives of this clinical investigation?

"The primary outcome for this 10-week medical trial is the total number of participants who completed. Secondary outcomes include PROMIS-29 scale score (1-5, higher scores indicating worse quality of life), Rand 36-Item Health Survey (SF-36) score (1-6, higher scores correlating with poorer health outcomes), and General Symptom Questionnaire (SGQ30) score(0 - 4, greater values pointing to severe symptomology)."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

Restoring Energy With Sub-symptom Threshold Optimized Rehabilitation Exercise for Long COVID

Annamaria R. Norweg 2023. "Restoring Energy With Sub-symptom Threshold Optimized Rehabilitation Exercise for Long COVID". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT06172803.

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