Digital Physical Activity Program

NCT07179796 | Enrolling By Invitation

• 1 other identifier: SH-OBS-MV-US-01
• Study Type: observational
• Target: 300,000
• Locations: 1 country
• Sites: 1

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.

Conditions

Overall Health; Wellbeing; Quality of Life; Mental Health

Outcome Measures

Primary Outcomes (1)

• Member Progress (PGIC)

  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.

  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.

Secondary Outcomes (17)

• Anxiety

  Assessed at baseline (upon initiation of the program) and then 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.

• Depression

  Assessed at baseline (upon initiation of the program) and then 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.

• Self-reported Quality of Life

  Assessed at baseline (upon initiation of the program) and then 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.

• Work productivity and absenteeism

  Assessed at baseline (upon initiation of the program) and then 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.

• Self-reported Fitness Level

  Assessed at baseline (upon initiation of the program) and then 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.

Other Outcomes (4)

• Sessions performed

  Through study completion, an average of 3 months

• Total Physical Activity Time

  Through study completion, an average of 3 months

• Average Physical Activity Time per Week

  Through study completion, an average of 3 months

Study Arms (1)

Observation

These programs will cover all participants interested in improving their health and wellness through increased physical activity.

Behavioral: Observation

Interventions

Observation BEHAVIORAL

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.

Observation

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

These programs will cover all participants interested in improving their health and wellness through increased physical activity.

You may qualify if:

• healthy individuals, or individuals with pre-existing conditions who are able to perform unsupervised exercise, unless contraindicated by their treating physician;
• older than the age of majority in their state of residence (US based);
• participant is able to understand study procedures and willing to provide informed consent.

You may not qualify if:

• younger than the age of majority in their state of residence;
• pain scores exceeds 6/10 on an 11-point numerical rating scale or member reports irregular movement patterns;
• undergone a surgical procedure within the last three months;
• presence of exertional red flags, as defined by the American College of Sports Medicine, and the participant has not been cleared to engage in an unsupervised exercise based program by their treating physician;
• health condition incompatible with an unsupervised exercise based program that has not been cleared by their treating physician;
• active cancer diagnosis, or is receiving treatment for cancer, and not been cleared by their treating physician to engage in an unsupervised exercise program;
• history of unexplained falls or utilization of an assistive device and has not been cleared by their treating physician to engage in an unsupervised exercise program;
• currently pregnant and has not been cleared by their treating physician to engage in an unsupervised exercise program;
• cognitive condition that prevents participant from understanding and independently executing an unsupervised exercise program.

Sponsors & Collaborators

• Sword Health, SA: lead

Study Sites (1)

Sword Health

New York, New York, 10016, United States

Location

MeSH Terms

Conditions

Psychological Well-Being

Interventions

Observation

Condition Hierarchy (Ancestors)

Personal Satisfaction; Behavior

Intervention Hierarchy (Ancestors)

Methods; Investigative Techniques

Study Officials

• Fernando D Correia, MD, PhD

  SWORD HEALTH INC

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 2 Years
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 10, 2025
• First Posted: September 18, 2025
• Study Start: September 9, 2025
• Primary Completion (Estimated): September 1, 2035
• Study Completion (Estimated): December 1, 2035
• Last Updated: September 18, 2025

Record last verified: 2025-09

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)