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Tirzepatide

Mounjaro, Zepbound, LY3298176

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Studies 183
Trials 100
Enrolling By Invitation OBSERVATIONAL NCT07179796

Digital Physical Activity Program

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

The purpose of this study is to create a research repository, composed of data collected during a digital physical activity program delivered by Sword Move to individuals undergoing those programs. Sword Move intends to increase physical activity levels to stimulate the adoption of healthier, more active lifestyles. This will allow investigators to observe the effects of participants' engagement in physical activity on a variety of health and wellness based outcomes.

Detailed Description

Purpose This patient registry was designed as a research repository, composed of data collected during a digital physical activity program delivered by Sword Move to individuals undergoing those programs. This data will allow the researchers to: 1. Assess the adoption, engagement and feasibility of digital physical activity programs to increase physical activity and its subsequent effect on health and wellness; 2. Assess the results of digital physical activity programs and compare the costs with the benefits obtained; 3. Correlate the results with patient's demographic and health condition profiles; Increase the knowledge regarding physical activity and its resultant effect on mental and physical health metrics; 4. Develop new or improved tools designed to help people improve physical activity levels and adopt healthier lifestyles. Design Prospective, observational study Study population These programs will cover all participants interested in improving their health and wellness through increased physical activity. Participants will be going through a personalized physical activity program tailored to each participant, with variations in frequency, duration, and type of activity based on their preferences, goals, fitness level, and physical ability. Outcomes The primary outcome will be the participant's progress along the program. Depending on the condition, primary and secondary outcome measures vary, but the registry will include, in all cases, a complete characterization of the participant's physical health status, as well as the periodic assessment of: a) performance indicators (through condition-specific tests); b) patient-reported outcomes (obtained using internationally validated pathology-specific questionnaires); c) compliance; d) patient satisfaction.

Interventions

Name: Observation
Type: BEHAVIORAL
Description: Personalized physical activity program tailored to each participant, with variations in frequency, duration, and type of activity based on their preferences, goals, fitness level, and physical ability.

Primary Outcomes

Measure: Member Progress (PGIC)
TimeFrame: Assessed at regular intervals (after 5, 9, 15, and every 6 days with activity until 3 months). Additional follow-up assessments may be undertaken at other times: 3, 6, and 12 months.
Description: Measured through the Patient Global Impression of Change (PGIC) questionnaire. Scores reflect the participant's perceived overall improvement (range 1-7), with higher scores indicating greater improvement.

Trial Information

NCT ID

NCT07179796

Status

Enrolling By Invitation

Study Type

OBSERVATIONAL

Sponsor

Sword Health, SA

Last Updated

December 15, 2025

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