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Not yet recruiting NCT07654868

CHARGE: Pilot Trial of Self-directed Use of Resources for Physical Activity

No phase Interventional Physical Activity

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: LLM alone, LLM enhanced, Sleep promotion.
Who it may be relevant to
Registry conditions: Physical Activity. Basic parameters: 18 years — 75 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 →

Overview

This is a pilot RCT examining physical activity outcomes at 3 months across 3 conditions: use of large language model (LLM) fully self-directed; use of LLM with guidance; and use of online tools to help with sleep.

Detailed description

To prepare for a future fully powered RCT, we are conducting a pilot RCT. The pilot RCT will enroll n=39 insufficiently active primary care patients, and randomize them to one of 3 conditions: LLM alone condition: participants are recommended to use a publicly available, general-purpose LLM for physical activity promotion over the next 3 months (n=13); LLM enhanced condition: participants are recommended to use a publicly available, general-purpose LLM for physical activity promotion over the next 3 months and additionally attend an initial session providing guidance on LLM use and weekly text message with suggestions on using the LLM (n=13); or Control condition: participants are recommended to use publicly available tools to help with sleep (websites with tips for sleep and guided meditation videos) over the next 3 months (n=13). At study onset, all participants will be given basic information about exercise safety. At 3 months, moderate-to-vigorous physical activity will be measured with a validated self-report measure. Feasibility and acceptability outcomes such as recruitment and retention--metrics essential for advancing to a subsequent large-scale trial-will be measured.

Interventions

  • Behavioral LLM alone
    Participants are recommended to use a publicly available, general-purpose LLM for physical activity promotion
  • Behavioral LLM enhanced
    Participants are recommended to use a publicly available, general-purpose LLM for physical activity promotion over the next 3 months and additionally attend an initial session providing guidance on LLM use and weekly text message with suggestions on using the LLM
  • Behavioral Sleep promotion
    Participants are recommended to use publicly available tools to help with sleep (websites with tips for sleep and guided meditation videos)

Primary outcome measures

  • Recruitment feasibility [Time frame: 6 months]
Secondary outcome measures (2)
  • Retention [Time frame: 3 month]
  • Physical activity [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • Age 18-75
  • Reports a desire to increase physical activity level
  • Not meeting minimum aerobic PA as indicated by L-CAT endorsement indicating level of activity below moderate (moderate defined as >= 5x/week activity or higher)
  • Reports willingness to use LLMs to help with exercise goals.
  • Access to internet through phone data plan or home Wi-Fi.

Exclusion criteria

  • Conditions warranting more extensive supervision of physical activity, including:
  • Any history of MI or stroke, arrhythmias, or heart failure
  • Uncontrolled hypertension
  • Type 1 or 2 diabetes
  • COPD or asthma
  • Recent orthopedic surgery or fracture
  • Advanced Parkinson's
  • Pregnant or planning to become pregnant in next 9 months
  • Active cancer undergoing treatment
  • Recent major surgery (<12 weeks)
  • Use of assistive devices for ambulation
  • History of eating disorder diagnosis
  • Dementia diagnosis
  • Unable to read on own.
  • Hospitalization for mental health reasons in past year
  • Has used LLM to support physical activity goals in prior 3 months.
  • Currently enrolled in a structured program to promote physical activity or weight loss.

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: NCT07654868 · IRB202600162

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗