Mobility Disability

8

Review clinical trials related to Mobility Disability. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Wearable Robotics to Overcome Exercise Dose Limitations in Older Adults - Study 2

The purpose of this research is to learn whether a lightweight wearable robotic device called We Innovate Mobility (WIM) can improve exercise capacity and physical function for older adults.

Participants needed: 32
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Wake Forest University Health SciencesUpdated: Oct 6, 2026Locations: 1
Eligibility criteria

Community-dwelling adult aged ≥65 years [+4]

Recent hospitalization, surgery, fracture, or other medical condition that limit... [+4]

Status: Recruiting

The Impact of Biological Mechanisms of Aging on Response Variability to Resistance Training in Older Adults

To critically examine biological, clinical, and behavioral modulators of progressive resistance training-associated exercise response heterogeneity in physical function and whole-body metabolism in older adults.

Participants needed: 300
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Mayo ClinicUpdated: Oct 5, 2026Locations: 2
Eligibility criteria

aged greater than or equal to 65 years [+4]

unwillingness to provide informed consent [+25]

Status: Not yet recruiting

Wearable Robotics to Overcome Exercise Dose Limitations in Older Adults - Study 1

The purpose of this research study is to learn whether a lightweight wearable robotic device called We Innovate Mobility (WIM) can improve exercise capacity and physical function for older adults.

Participants needed: 16
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Wake Forest University Health SciencesUpdated: Oct 5, 2026Locations: 1
Eligibility criteria

Community-dwelling adult aged ≥65 years [+4]

Recent hospitalization, surgery, fracture, or other medical condition that limit... [+5]

Status: Not yet recruiting

Reduction of Anxiety Through Dual Treatment: Digital CBT & NBHWC Coaching

The purpose of this study is to see if a mobile-delivered mental health program called Toivoa-001, which combines digital cognitive behavioral therapy (CBT) with personal mental health coaching, can effectively reduce anxiety in adults with hearing or mobility disabilities. The study aims to answer whether this dual-intervention digital service is more effective at lowering anxiety symptoms over an 8-week period than a "sham" digital program that is developed to look similar but does not contain active therapeutic content. The investigators hypothesize that participants who use the Toivoa-001 program will show significantly greater reductions in anxiety compared to those using the sham program, and that these mental health benefits will last through a 12-week follow-up. Adults within the disability community frequently encounter unique environmental and societal barriers - such as limited physical accessibility, transportation challenges, and workplace inflexibility - that can directly drive or worsen anxiety. By offering a fully remote and accessible mobile tool, this study seeks to determine if a digital health service can deliver scalable, effective anxiety relief tailored to the lived experiences of people with disabilities.

Participants needed: 200
Trial details
Age: 22+Biological sex: AllType: InterventionalSponsor: Toivoa IncUpdated: Sep 14, 2026Locations: 4
Eligibility criteria

Provision of signed and dated informed consent form [+10]

Medical diagnosis of psychotic disorder or bipolar disorder [+4]

Status: Not yet recruiting

Reduction of Depression Through Dual Treatment: Digital CBT & NBHWC Coaching

The purpose of this study is to see if a mobile-delivered mental health program called Toivoa-002, which combines digital cognitive behavioral therapy (CBT) with personal coaching, can effectively reduce depression in adults with hearing or mobility disabilities. The study aims to answer whether this dual-intervention digital service is more effective at lowering depression symptoms over an 8-week period than a "sham" digital program that is developed to look similar but does not contain active therapeutic content. The investigators hypothesize that participants who use the Toivoa-002 program will show significantly greater reductions in depression compared to those using the sham program, and that these mental health benefits will last through a 12-week follow-up. Adults within the disability community frequently encounter unique environmental and societal barriers - such as limited physical accessibility, transportation challenges, and workplace inflexibility - that can directly drive or worsen depression. By offering a fully remote and accessible mobile tool, this study seeks to determine if a digital health service can deliver scalable, effective depression relief tailored to the lived experiences of people with disabilities.

Participants needed: 200
Trial details
Age: 22+Biological sex: AllType: InterventionalSponsor: Toivoa IncUpdated: Sep 10, 2026Locations: 4
Eligibility criteria

Provision of signed and dated informed consent form [+10]

Medical diagnosis of psychotic disorder or bipolar disorder [+4]

Status: Not yet recruiting

Impact of Loss Aversion Messaging and Anticipated Regret for Inaction on Exercise Adherence in Older Adults

The goal of this clinical trial is to learn if messages focused on not losing the functional benefits of exercise can help older adults with walking difficulty continue to exercise regularly. The main questions it aims to answer are: Do these messages make people more likely to anticipate regretting it if they do not exercise? Does more anticipated regret make it more likely they will exercise more regularly? Researchers will compare two versions of messages to see if the content of these one of these message types is more effective than the other. Participants will complete a daily 5-minute at home exercise program for 4 months and complete regular online surveys to track their progress and report their feelings regarding regret.

Participants needed: 148
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Milton S. Hershey Medical CenterUpdated: Aug 12, 2026Locations: 1
Eligibility criteria

Completed 12 months of FAST intervention

No planned surgeries within the upcoming 4 months

Status: Recruiting

Home-Based Brain Stimulation for Motoric Cognitive Risk Syndrome

The objective of this study is to determine the effects of a 6-month, home-based personalized transcranial direct current stimulation (tDCS) intervention targeting the left dorsolateral prefrontal cortex on cognitive function, dual task standing and walking, and other metrics of mobility in older adults with motoric cognitive risk syndrome (MCR).

Participants needed: 128
Trial details
Age: 65-90Biological sex: AllType: InterventionalSponsor: Hebrew SeniorLifeUpdated: Jul 16, 2026Locations: 2
Eligibility criteria

Men and women [+8]

Formal education less than the 8th grade [+19]

Status: Recruiting

Cocoa to Maximize Exercise Training in Older Adults - The COMET Trial

The purpose of the study is to see if regular exercise when combined with a cocoa supplement will improve physical performance and muscle strength compared to regular exercise alone.

Participants needed: 36
Trial details
Phase: Phase 1, Phase 2Age: 55+Biological sex: AllType: InterventionalSponsor: University of Alabama at BirminghamUpdated: May 8, 2026Locations: 1
Eligibility criteria

Age 55 years and older [+3]

Failure to provide informed consent; [+15]