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Not yet recruiting NCT07535918

Using e-Technologies to Maximize Physical Activity After Cancer Treatment

No phase Interventional Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Cancer Exercise App.
Who it may be relevant to
Registry conditions: Cancer. Basic parameters: 18 years — 85 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Using e-Technologies to Maximize Physical Activity After Cancer Treatment: The eMPACT Trial

Overview

The Cancer Exercise app (CEA) is designed to promote physical activity among cancer survivors. The proposed randomized controlled clinical trial will investigate, in adults who have completed cancer treatment, the effects of a 12-week home-based exercise program, delivered using CEA, on physical activity levels. Participants will be randomized into one of two groups: (1) CEA or (2) Usual Care.

Interventions

  • Behavioral Cancer Exercise App
    Use of Cancer Exercise app to increase physical activity levels among cancer survivors.

Primary outcome measures

  • Change in moderate to vigorous physical activity from pre- to post-intervention [Time frame: Baseline and following the 12-week intervention]

Eligibility criteria

Inclusion criteria

  • 18 to 85 years of age
  • Diagnosed with stage I-III cancer
  • Completed all primary cancer treatments (e.g., surgery, radiation, chemotherapy) at least 6 months prior to enrollment. Adjuvant endocrine therapy, CDK4/6 inhibitors, PARP inhibitors, immunotherapy, and bisphosphonates are allowed within 6 months of study enrolment and during study participation.
  • Own a smartphone with data plan or access to WiFi (Apple or Android)
  • Medical clearance provided or no medical clearance needed based on exercise preparticipation screening.

Exclusion criteria

  • consistently engage in >300 min/week of moderate-intensity physical activity or 150 min/week of vigorous-intensity physical activity in the past 3 months
  • receiving or scheduled to receive surgery or radiation during study participation
  • have stage IV metastatic cancer or evidence of cancer recurrence
  • have multiple myeloma
  • have received bone marrow or hematopoietic stem cell transplant within past year
  • are unable to walk without support or have severe weakness or balance problems that limit safe participation in exercise
  • contraindications to participate in unsupervised exercise
  • are pregnant
  • unable to read, speak and understand English

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Prevention

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07535918 · IRB202501619

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗