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Completed

NCT Number: NCT05205512

Telehealth Exercise Intervention to Improve Cardiovascular Health in Lymphoma Survivors, TECHS Trial

This clinical trial tests how well a telehealth exercise intervention works to improve cardiovascular health in lymphoma survivors. Telehealth exercise is a service to help perform physical exercises at home with a care provider online. With the use of telehealth exercise lymphoma survivors may be able to participate in exercise programs safely to improve heart health and reduce the risk of cardiovascular disease.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

City of Hope Medical Center

Duarte, California, 91010, United States

About this study

PRIMARY OBJECTIVE:

I. Determine the feasibility of an 8-week telehealth exercise intervention, as assessed by enrollment, retention, and adherence to the telehealth exercise intervention.

SECONDARY OBJECTIVE:

I. Explore the effects of an 8-week telehealth exercise intervention on cardiovascular health, assessed by cardiopulmonary exercise test, pulmonary function test, body compositions, and blood biomarkers.

OUTLINE: Participants are randomized into 1 of 2 groups.

GROUP I (TELEHEALTH EXERCISE): Patients participate in telehealth exercise intervention for 30 minutes per day, 3 days a week for 8 weeks.

GROUP II (DELAYED CONTROL): Patients maintain current levels of physical activity for 8 weeks. Patients may then participate in telehealth exercise intervention for 8 weeks.

After completion of study treatment, participants are followed up after 1 week.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed with Hodgkin or non-Hodgkin lymphoma.
  • >= 18 years old.
  • Are between 2-5 years after completing anti-cancer therapy and with no evidence of disease.
  • Intermediate (4-5) to high ( >= 6) risk of cardiovascular risk factors based on six key variables: Age 30 to 50 years (y) [2]) and >= 50y [3]; anthracycline dose >250mg/m ^ 2 [1]; hypertension [2]; diabetes [2]; smoking [1]; and chest radiation [1]).
  • Able to understand and sign the informed consent document.
  • Physically able and willing to complete all study procedures.

Exclusion criteria

  • Have overt cardiovascular disease within 6 months (e.g. myocardial infarction, stroke, angina).
  • Have contraindications to exercise.
  • Participate in structured exercise (>60 minutes/week).
  • Female patients who are pregnant or planning to become pregnant.

Treatment and study plan

Exercise intervention

Other

Maintain current levels of physical activity

Questionnaire Administration

Other

Ancillary studies

Telemedicine

Other

Participate in telehealth exercise intervention

Other names: Telehealth

Primary outcomes

  1. Adherence to the telehealth exercise intervention

    Time frame: Up to 2 years

    Adherence will be measured by the number of exercise sessions attended over the exercise sessions prescribed (17/24 sessions).

Secondary outcomes

  1. Effects of an 8-week telehealth exercise intervention

    Time frame: At baseline up to week 9

    The physiologic effects of telehealth exercise intervention will be assessed by peak oxygen consumption (VO2) using cardiopulmonary exercise testing.

Sponsors and collaborators

Lead sponsor

City of Hope Medical Center

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

Telehealth Exercise Intervention to Improve Cardiovascular Health in Lymphoma Survivors (TECHS): A Pilot Feasibility Study

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Jan 25, 2022
Registry last updated
Oct 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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