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

RECRUITING NA

Improving Exercise Capacity With a Tailored Physical Activity Intervention

NCT05595577 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this research is to test whether participating in either a physical activity intervention or a series of educational classes will help to preserve exercise capability, heart function, brain-based activities (like memory), and quality of life. Participants will be randomized to 1 of 2 pathways: * First pathway consists of organized health workshops. These workshops are intended to provide information on topics such as proper nutrition, management of stress, sleep practices, and emphasis on a healthy lifestyle that may help the participants through cancer treatment. This pathway will also test whether stretching may help participants through cancer treatment. * Second pathway participants will take part in some unsupervised and some potentially supervised moderate activity sessions each week throughout participants' cancer treatment to take place either remotely or in person, depending on availability of facilities at the time visits are scheduled.

Interventions

  • BEHAVIORAL Quality of Life Questionnaires
  • OTHER Exercise with Trainerize application
  • DIAGNOSTIC_TEST Cardiopulmonary exercise testing
  • DIAGNOSTIC_TEST MRI scan
  • BEHAVIORAL Cognitive and Brain Function Questionnaires

Study Locations (2)

North Carolina

  • Wake Forest Baptist Comprehensive Cancer Center — Winston-Salem

Virginia

  • Virginia Commonwealth University — Richmond

Trial Details

FieldValue
Enrollment Target 110 participants
Start Date 2023-03-01
Est. Completion 2026-08-31
Phase NA

Sponsor

Wake Forest University Health Sciences

1,061 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05595577

The ClinicalTrials.gov registry entry for NCT05595577 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,061 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 7 conditions, with Quality of Life appearing as the primary indexed condition, and to 5 interventions — of which Quality of Life Questionnaires is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05595577 reports 2 study locations spanning 2 distinct geographic areas — top geographies include North Carolina, Virginia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05595577 about?

NCT05595577 is a clinical study titled "Improving Exercise Capacity With a Tailored Physical Activity Intervention". The purpose of this research is to test whether participating in either a physical activity intervention or a series of educational classes will help to preserve exercise capability, heart function, brain-based activities (like memory), and quality of life. Participants will be randomized to 1 of 2...

What is the current status of trial NCT05595577?

This trial is currently recruiting. It is a NA study. The enrollment target is 110 participants. The study started on 2023-03-01. Estimated completion is 2026-08-31.

What conditions does trial NCT05595577 study?

This clinical trial studies the following conditions: Quality of Life, Hodgkin Lymphoma, Non Hodgkin Lymphoma, Stage II Breast Cancer, Stage III Breast Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05595577?

The interventions under investigation include: Quality of Life Questionnaires (BEHAVIORAL), Exercise with Trainerize application (OTHER), Cardiopulmonary exercise testing (DIAGNOSTIC_TEST), MRI scan (DIAGNOSTIC_TEST), Cognitive and Brain Function Questionnaires (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05595577?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,061 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05595577 being conducted?

This trial has 2 study locations across North Carolina, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial