What side effects are associated with this type of intervention?

The most common treatments for sedentary lifestyle that leverage social networking and geotagging, such as the Person-Centered Geotagged Social Networking System (SNS), generally have minimal physical side effects. However, potential side effects may include digital fatigue, privacy concerns, and the risk of misinformation. Users might experience digital fatigue due to prolonged screen time and constant notifications. Privacy concerns arise from sharing personal location and activity data. Additionally, the spread of misinformation or unverified information about physical activity resources can lead to confusion or misuse. Overall, these interventions are well-tolerated and can effectively promote physical activity with proper management of these side effects.

What prior FDA approvals exist?

As of now, there are no specific FDA-approved drugs for the treatment of a sedentary lifestyle. However, various digital health interventions, including mobile apps and online platforms, have been studied for their effectiveness in promoting physical activity. These interventions often use principles of social networking and geotagging to enhance user engagement and provide information about accessible physical activity resources. While these digital tools are not FDA-approved as treatments, they are increasingly recognized for their potential to address sedentary behavior and improve overall health.

What other types of research exist?

Promising, novel alternatives for sedentary lifestyle patients in 2024 include: 1) Mobile apps that provide personalized exercise plans and track physical activity, such as MyFitnessPal or Fitbit. 2) Online platforms that offer virtual fitness classes and community support, like Peloton or Daily Burn. 3) Telehealth interventions that connect patients with fitness coaches and healthcare providers for remote guidance and support. 4) Wearable devices that monitor physical activity and provide real-time feedback, such as Apple Watch or Garmin. These alternatives leverage technology to promote physical activity and provide accessible resources and support for patients.

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Geotagged Social Networking for Physical Disabilities (RECTECHIV Trial)

N/A

Recruiting

Research Sponsored by University of Alabama at Birmingham

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Self-reported physical disability that limits their mobility

18 to 64 years old

Must not have

Ongoing exacerbation of a health condition

Severe pulmonary disease or renal failure

Timeline

Screening 3 weeks

Treatment Varies

Follow Up pre-intervention and again at the end of 12 weeks

Awards & highlights

No Placebo-Only Group

Summary

This trial tests a new online resource called RecTech Match, designed to help people with physical disabilities find accessible exercise opportunities. The goal is to reduce barriers and increase physical activity by providing tailored resources and support.

Who is the study for?

This trial is for people aged 18 to 64 with a self-reported physical disability that limits their mobility. It's not suitable for those who have trouble understanding instructions due to cognitive or linguistic issues, are currently pregnant, had a recent cardiovascular event, have severe pulmonary disease or renal failure, or any health condition exacerbation.

What is being tested?

The trial is testing the RecTech Match Website – a social networking system designed to help individuals with physical disabilities find accessible community-based exercise and recreation programs by overcoming various barriers.

What are the potential side effects?

Since this intervention involves using a website rather than taking medication or undergoing medical procedures, traditional side effects are not applicable. However, users may experience frustration if technical issues arise or if desired information isn't easily found.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

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I have a physical disability that limits my ability to move around.

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I am between 18 and 64 years old.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:

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I am currently experiencing a worsening of my health condition.

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I do not have severe lung or kidney disease.

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I don't have conditions that stop me from being active.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ pre-intervention and again at the end of 12 weeks

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~pre-intervention and again at the end of 12 weeks

This trial's timeline: 3 weeks for screening, Varies for treatment, and pre-intervention and again at the end of 12 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.

Primary study objectives

Barriers to Physical Activity Questionnaire for People with Mobility Impairments

Chogahara's Social Influence on Physical Activity Questionnaire

Godin - Leisure time physical activity questionnaire

+1 more

Secondary study objectives

FitBit device data (total energy expenditure, steps, sedentary time, light activity time, moderate activity time, high activity time, and activity energy expenditure).

Awards & Highlights

No Placebo-Only Group

All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups

Experimental Treatment

Active Control

Group I: interventionExperimental Treatment1 Intervention

The intervention group will be mailed a Fitbit device and provided access to the RecTech Match website. Intervention participants will receive weekly calls for the first 6 weeks, and a call every other week for the following 6 weeks (9 in total) from a health coach to discuss progress, facilitate setting physical activity goals, and help mitigate obstacles to participate in physical activity in the community. Participants will be free to access the features and resources of the website. The Fitbit data will be collected on an ongoing basis and the participants will receive daily texts asking them to rate the amount of physical activity for the day.

Group II: ControlActive Control1 Intervention

The control participants will not have access to the RecTech Match website; however, control participants will be directed to generic information available on the NCHPAD website, which includes the same information but is not delivered through RecTechMatch.com.

0 / 5Eligibility criteria met

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.

Mechanism Of Action

Side Effect Profile

Prior Approvals

Other Research

Common treatments for sedentary lifestyle, such as the Person-Centered Geotagged Social Networking System (SNS), leverage social networking and geotagging to identify and share information about accessible physical activity resources. These interventions work by addressing multilevel barriers to physical activity, providing real-time, location-based information, and fostering a supportive community environment. This matters for sedentary lifestyle patients as it enhances motivation, reduces barriers to exercise, and promotes sustained engagement in physical activities through social support and easy access to local resources.

Feasibility of a social media-based weight loss intervention designed for low-SES adults.Twitter-Based Social Support Added to Fitbit Self-Monitoring for Decreasing Sedentary Behavior: Protocol for a Randomized Controlled Pilot Trial With Female Patients From a Women's Heart Clinic.Effects of Social Network Exposure on Nutritional Learning: Development of an Online Educational Platform.