Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Effects of X Box Kinect 360 in Alzheimer's Disease

Alzheimer's disease (AD) is a progressive neurodegenerative disorder and the most common cause of dementia that accounting for 60% to 80% of all cases (Better, et al., 2023). According to world health organization (WHO), more than 55 million people globally live with dementia, and this number is expected to rise to 78 million by 2023 and 139 million by 2050 (WHO, 2021).

Participants needed: 38
Trial details
Age: 50-85Biological sex: AllType: InterventionalSponsor: Ziauddin UniversityUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Alzheimer's disease of age between 50-85 years. [+1]

Undiagnosed AD patients. [+1]

Status: Not yet recruiting

Virtual Reality Training Using Wii Fit in Children With Cerebral Palsy

The goal of this clinical trial is to determine whether virtual reality (VR) training using the Nintendo Wii Fit can improve balance, gross motor function, and agility in children aged 7-14 years with spastic cerebral palsy (GMFCS Levels I-II). The main questions it aims to answer are: Does Wii Fit-based VR training improve balance more than conventional physiotherapy? Does VR training enhance gross motor skills such as standing, walking, running, and jumping? Does VR training improve agility in children with cerebral palsy? Does VR training increase enjoyment and engagement during therapy? Researchers will compare Wii Fit-based VR training with conventional physiotherapy to determine which approach leads to greater improvements in motor function. Participants will: Attend 18 sessions over 6 weeks (3 sessions per week). Perform either VR-based exercises using the Wii Fit Balance Board or traditional physiotherapy exercises. Complete pre- and post-intervention assessments using the Pediatric Balance Scale, GMFM-88 (domains D and E), BOT-2 agility subtest, and the PACES enjoyment scale. This study aims to explore a fun, cost-effective, and engaging rehabilitation strategy that may improve functional independence and overall quality of life for children with cerebral palsy.

Participants needed: 56
Trial details
Age: 7-14Biological sex: FemaleType: InterventionalSponsor: Ziauddin UniversityUpdated: Apr 23, 2026
Eligibility criteria

● Children aged 7 to 14 years [+6]

● Orthopedic surgery or botulinum toxin injections in the past 16 months [+3]

Status: Not yet recruiting

Effect of Biofeedback-Enhanced Exergaming, Exergaming Alone, and Traditional Physical Therapy on Motor Function, Adherence, and Engagement in Children With Cerebral Palsy: A RCT

Cerebral Palsy (CP) accounts for approximately 0.9% of the global disease burden and affects 2.4-4% of children under 5 years old, with associated developmental and coordination impairments. Pediatric physical therapy aims to enhance independence and quality of life; however, maintaining adherence to conventional treatment remains a major challenge due to its repetitive and monotonous nature, leading to reduced motivation and limited functional progress. Exergaming, integrating physical activity with interactive video games, has emerged as an engaging alternative shown to improve motor function, balance, and coordination in children with motor impairments. While existing evidence supports its effectiveness, few randomized studies have explored the addition of real-time physiological biofeedback (e.g., surface EMG with motion tracking) within exergaming platforms. Evidence on adherence and engagement outcomes also remains limited. This trial addresses that gap by investigating the combined effects of biofeedback-enhanced exergaming versus exergaming alone and traditional physiotherapy in children with CP (GMFCS levels I-II). Incorporating real-time biofeedback provides immediate physiological feedback, potentially enhancing motor learning, motivation, and adherence, key components for improving long-term rehabilitation outcomes in pediatric populations.

Participants needed: 90
Trial details
Age: 6-12Biological sex: AllType: InterventionalSponsor: Ziauddin UniversityUpdated: Jan 8, 2026Locations: 1
Eligibility criteria

Gross Motor Function Classification System (GMFCS) Level I or II. [+7]

GMFCS Level III or higher, indicating significant gross motor limitations. [+7]

Status: Not yet recruiting

An Investigation of the Efficacy of OHEM for Improving Oral Hygiene in Children

This pilot study evaluates the feasibility of conducting a larger Randomized Controlled Trial to compare three oral health education delivery methods to a control group. Except for the control group, mothers in the three intervention groups will receive the same oral health education based on the OHEM module but differ in the delivery methods, namely lecture, exhibition, and demonstration. All groups will receive a booklet and oral hygiene kits and be instructed to educate their children at home. Pre- and post-intervention assessments include the satisfaction of participants, the researchers' evaluation and cost of the trial, oral hygiene status, and the knowledge of the parents and children.

Participants needed: 540
Trial details
Age: 12-40Biological sex: AllType: InterventionalSponsor: Ziauddin UniversityUpdated: Jul 24, 2024Locations: 1
Eligibility criteria

Mothers with children aged 12 to 15 years old, who are residing in Gulshan-e-Sik... [+2]

Mothers with new-born [+7]