Sensory Processing Disorder

6

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

Condition / disease
Location
Status: Not yet recruiting

Ayres Sensory Integration Test Evaluation Results and Neurodevelopmentally Focused Counseling in Children With Neurodevelopmental Problems

The aim of the study is to investigate the long-term effects of ASI-based and hybrid neurodevelopmental counseling services on the variables of the Ayres Sensory Integration Assessment Test in children with neurodevelopmental disorders.

Participants needed: 16
Trial details
Age: 3-12Biological sex: AllType: ObservationalSponsor: Yeditepe UniversityUpdated: Jun 18, 2026Locations: 1Duration: 1 Month
Eligibility criteria

Aged 3-12 [+7]

Being under 3 years of age or over 12 years of age [+1]

Status: Recruiting

Ayre's Sensory-Motor Integration Exercises and Sensory Modulation And Motor Skills In Children With ASD

This study will adopt a quasi-experimental design, featuring assessments before and after the intervention for both the experimental and control groups. We plan to recruit thirty children aged 9 to 11 years, all diagnosed with ASD, from a local clinical setting. Participants will be randomly assigned to either a treatment group, which will undergo 12 sessions of sensory-motor integration exercises, or a control group that will receive standard care. Each session will include structured sensory-based activities based on Ayres Sensory Integration® principles.

Participants needed: 28
Trial details
Age: 9-11Biological sex: AllType: InterventionalSponsor: Riphah International UniversityUpdated: May 8, 2026Locations: 1
Eligibility criteria

Diagnosis of Autism Spectrum Disorder (ASD) confirmed by a psychiatrist/psycholo... [+2]

Use of any sedative/hypnotic drugs. [+2]

Status: Not yet recruiting

Chiropractic for Kids With Sensory Processing Challenges

The main aim of this pilot observational study is to investigate the feasibility of implementing our novel assessment battery in tandem with normal and customary chiropractic care in a practice-based setting using a pediatric population with parent-reported sensory processing disorder (SPD). The secondary aim is to assess potential changes in objective and subjective outcomes.

Participants needed: 20
Trial details
Age: 5-12Biological sex: AllType: ObservationalSponsor: Life UniversityUpdated: May 8, 2026Locations: 1
Eligibility criteria

5-12 years of age. [+1]

A known heart condition, including pacemakers [+1]

Status: Recruiting

Sensory and Cognitive Predictions, and Their Disruptions in Schizophrenia

Disturbances in the sense of self and time could play an important role in the development of psychotic symptoms. Previous work has shown that patients have difficulty preparing to process information on the scale of a second, but are abnormally disturbed by slightly asynchronous information on the millisecond scale. In both cases, the anomalies could explain the patients' unusual experience of time. The hypothesis in neurotypical patients is that small delays or asynchronies asynchronies are treated as irrelevant information and ignored and ignored, whereas in patients suffering from schizophrenia they would disrupt the flow of time. This hypothesis is tested with a new visual illusion.

Participants needed: 68
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Centre Psychothérapique de NancyUpdated: Mar 25, 2026Locations: 2
Eligibility criteria

Male or female; [+3]

Psychoactive substance use disorders (as defined by the DSM-V) (Diagnostic and S... [+8]

Status: Recruiting

Intensive Multimodal Neurorehabilitation Targeting Neuroplasticity in Pediatric Neurodevelopmental and Chromosomal Disorders

This observational study evaluates functional and developmental outcomes in pediatric participants undergoing a two week intensive multimodal neurorehabilitation program. The program is designed for children with neurodevelopmental disorders, including but not limited to cerebral palsy, autism spectrum disorder, developmental delay, hypoxic ischemic encephalopathy (HIE), and chromosomal or genetic abnormalities. Participants receive individualized therapy sessions for approximately 2.5 hours per day over a two week period. The intervention is not standardized but is tailored to each child's specific needs and may include components such as sensory integration, motor planning, reflex integration, oculomotor training, executive functioning activities, communication support, and other brain based therapeutic approaches. The purpose of this study is to observe changes in functional abilities, including attention, motor coordination, emotional regulation, communication, and activities of daily living. Outcomes are assessed using clinician observation and parent reported changes before and after the intensive program, with limited follow-up when available. This study does not assign participants to a specific treatment as part of a research protocol. Instead, it collects real world data from children already participating in a clinical therapy program to better understand potential benefits of intensive, individualized neurorehabilitation approaches.

Participants needed: 100
Trial details
Age: 4-12Biological sex: AllType: ObservationalSponsor: Healing Hope InternationalUpdated: Mar 25, 2026Locations: 1
Eligibility criteria

Pediatric participants between approximately 4 and 12 years of age at the time o... [+17]

Medical instability or acute medical condition that would prevent safe participa... [+5]

Status: Recruiting

Who and Why do Patients Report Lymphedema After Breast Cancer Treatment Without an Objective Measurable Swelling

Breast cancer related lymphedema (BCRL) at the arm and/or trunk is an extremely dreaded complication after breast cancer treatment due to its chronicity and impact. The incidence of objective arm and trunk/ breast BCRL is declining due to the major shift into the treatment approach of breast cancer. However, many patients report a sensation of swelling without the presence of objective BCRL, referred to as subjective BCRL. Therefore, subjective BCRL is defined as the diagnosis of BCRL based on the patient's sensation of a difference in size at the arm and/or trunk without the presence of objective BCRL. At this moment, there is no clear information on the prevalence and the transitions between different BCRL states (no-subjective-objective) over time, as well as about the underlying mechanisms and contributing factors of subjective BCRL. Therefore, the investigators hypothesize that four mechanisms might be associated with the presence and severity of subjective arm or trunk/breast BCRL, including the presence and/ or severity of lymphatic (1) and sensory processing problems (nociceptive (2), neuropathic (3), and/or central sensory processing problems (4)). The investigators will set up a prospective longitudinal study with breast cancer patients to determine the prevalence of subjective and objective arm or trunk/ breast BCRL at 1, 6, and 12 month(s) post-surgery and the transitions between different BCRL states (no-subjective-objective BCRL) (AIM 1). In addition, factors related to four potential underlying mechanisms (lymphatic, nociceptive, neuropathic, and central sensory processing problems) that contribute to the occurrence of subjective BCRL in comparison to no self-reported swelling and objective BCRL will be determined (AIM 2). Furthermore, the present study will be undertaken to determine factors related to these four underlying mechanisms that contribute to the severity of subjective BCRL at arm or trunk/ breast BCRL within the group of patients with subjective BCRL at different time-points after surgery (at 1, 6, and 12 month(s) post-surgery) (AIM 3).

Participants needed: 230
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Universitaire Ziekenhuizen KU LeuvenUpdated: Jan 29, 2025Locations: 1
Eligibility criteria

adults (men and women) who are ≥ 18 years of age [+4]

distant metastases [+4]