Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05658536 · ClinicalTrials.gov registry record · NA

The COPE Study: Pilot Intervention to Improve Symptom Self-management and Coping in Adults With Post COVID-19

A NA study, sponsored by University of Washington.

Completed
Registry status
NA
Development phase
51
Enrollment target

NCT05658536: Completed NA study, sponsored by University of Washington.

NCT05658536 is a NA study that has completed, run by University of Washington. The registered enrollment target is 51 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05658536, a NA study, has completed, sponsored by University of Washington.

COMPLETED
Registry status
NA
Development phase
51 participants
Enrollment target

Study Summary

This project is a randomized controlled pilot trial using mixed methods to examine the feasibility, acceptability, and initial effects of a telemedicine group-based intervention designed to improve symptom management and coping in adults with Post-COVID.

Primary Outcome

Intervention Acceptability will be measured with the Acceptability of Intervention Measure (AIM). When assessed via online survey, responses from the Intervention Acceptability items will be averaged to create an average score \[1-5\]. A higher score indicates more agreement with intervention acceptability while a lower score indicates less agreement with intervention acceptability.

Interventions

  • BEHAVIORAL 6-Week Self-Management Group

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2023-01-18
Est. Completion 2024-01-30
Phase NA
University of Washington

1,048 total trials

What the finished NCT05658536 record still lists

NCT05658536 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which 6-Week Self-Management Group is the first listed.

NCT05658536 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05658536 about?

NCT05658536 is a clinical study titled "The COPE Study: Pilot Intervention to Improve Symptom Self-management and Coping in Adults With Post COVID-19". This project is a randomized controlled pilot trial using mixed methods to examine the feasibility, acceptability, and initial effects of a telemedicine group-based intervention designed to improve symptom management and coping in adults with Post-COVID.

What is the current status of trial NCT05658536?

This trial is currently completed. It is a NA study. The enrollment target is 51 participants. The study started on 2023-01-18. Estimated completion is 2024-01-30.

What interventions are being tested in trial NCT05658536?

The interventions under investigation include: 6-Week Self-Management Group (BEHAVIORAL).

Who is sponsoring clinical trial NCT05658536?

This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05658536's enrollment target sits among peer trials

51 1279th of 2000 higher than 722 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02701153 · 51 participants · NA

    Phase II Study of 5-Day Hypofractionated Preoperative Radiation Therapy for Soft Tissue Sarcomas: Expansion Cohort

  • NCT03663790 · 51 participants · NA

    Effects of Gait Retraining on Lower Extremity Biomechanics

  • NCT03874052 · 51 participants · Phase 1

    Ruxolitinib in Combination With Venetoclax With and Without Azacitidine in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia

  • NCT04704661 · 51 participants · Phase 1

    Testing the Combination of Two Anti-cancer Drugs, DS-8201a and AZD6738, for The Treatment of Advanced Solid Tumors Expressing the HER2 Protein or Gene, The DASH Trial

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05658536, the US trial registry maintained by the National Library of Medicine. NCT05658536 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.