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Rehabilitation clinical trials

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NCT ID: NCT06085911 Not yet recruiting - Rehabilitation Clinical Trials

RCT Long COVID-19 Rehabilitation

Start date: November 2023
Phase: N/A
Study type: Interventional

The Coronavirus 2019 (COVID-19) pandemic has resulted in at least four million infections in Norway. The vast majority of cases are diagnosed and followed up in the community, but some with extensive symptoms and large degree of reduced function are referred to regional Covid-clinics. In total this patient group is placing an enormous burden on the already over stretched health care services. As the pandemic subsides the emerging threat of long-term disability from COVID remains to be quantified. Brain fog and cognitive symptoms are common in long COVID in 30% of mild infections resulting in sick leave and loss of daily function, with women overrepresented among long COVID sufferers. The true prevalence and underlying mechanisms of long COVID remains to be quantified. Although vaccination prevents severe infection and death, we have little knowledge on how best to rehabilitate those who suffers from long COVID. Here we propose to develop knowledge on treatment interventions to counteract disability from long COVID and lessening the burden on health care services. We will conduct a study of where we compare a short group intervention with systematic personalised neurocognitive rehabilitation to document symptom alleviation. Our overarching goal is to develop effective programmes for this evolving disease to reduce the suffering for the patients, and thereby reducing costs for health services and society at large.

NCT ID: NCT06075381 Not yet recruiting - Clinical trials for Postoperative Complications

Pulmonary Expansion Device in Tracheostomized Patients Therapies in Tracheostomized Patients

PEDTRAQ
Start date: February 2024
Phase: Phase 2
Study type: Interventional

The goal of this clinical trial is to evaluate the safety and efficacy of using PED (Pulmonary Expansion Device) in tracheostomized patients requiring lung reexpansion therapy within a single institution. The main question it aims to answer is: In tracheostomized patients requiring lung reexpansion therapy, does the utilization of PED (Pulmonary Expansion Device) alongside conventional management constitute a safe and effective strategy for improving oxygenation, lung volumes, and reducing postoperative pulmonary complications, as compared to traditional management alone? Researchers will compare lung expansion therapy with PED plus conventional management versus lung expansion therapy through conventional management in tracheostomized patients to assess the safety and efficacy in terms of improvement in oxygenation, lung volumes, and reduction of postoperative pulmonary complications.

NCT ID: NCT05958433 Not yet recruiting - Rehabilitation Clinical Trials

Preoperative Rehabilitation With Stoma Appliance in Colorectal Cancer Patients

Start date: August 2023
Phase: N/A
Study type: Interventional

This is a randomized, controlled trial aiming to assess the effects of preoperative education using stoma appliance on stoma self-care, quality of life, anxiety, and depression levels in colorectal cancer patients with a stoma.

NCT ID: NCT05957289 Not yet recruiting - Quality of Life Clinical Trials

Multidimensional Rehabilitation Intervention in Colorectal Cancer Survivors - a Pilot Study

Start date: June 1, 2024
Phase: N/A
Study type: Interventional

A metaverse-based multidimensional rehabilitation program will be implemented for colorectal cancer survivors who have undergone curative surgery and adjuvant therapy. The intervention is based on the behavior change wheel and includes dietary intervention, exercise intervention, psychological support, and behavior management. Through various methods such as training, education, and motivation, the program aims to enhance the patients' functional ability, opportunities, and motivation, thereby promoting healthy behavior. Outcome measures include quality of life, fear of recurrence, and adoption of a healthy lifestyle. The intervention period is 4 weeks, with evaluations conducted at baseline and week 4 of the intervention.

NCT ID: NCT05956990 Not yet recruiting - Quality of Life Clinical Trials

Multidimensional Rehabilitation Intervention in Colorectal Cancer Survivors

Start date: July 1, 2024
Phase: N/A
Study type: Interventional

A metaverse-based multidimensional rehabilitation program will be implemented for colorectal cancer survivors who have undergone curative surgery and adjuvant therapy. The intervention is based on the behavior change wheel and includes dietary intervention, exercise intervention, psychological support, and behavior management. Through various methods such as training, education, and motivation, the program aims to enhance the patients' functional ability, opportunities, and motivation, thereby promoting healthy behavior. Outcome measures include quality of life, fear of recurrence, and adoption of a healthy lifestyle. The intervention period is 4 weeks, with evaluations conducted at baseline and week 4 of the intervention

NCT ID: NCT05898542 Not yet recruiting - Stroke Clinical Trials

Nature-based Therapies in Stroke Rehabilitation

Start date: May 31, 2023
Phase: N/A
Study type: Interventional

Stroke rehabilitation patients are subjected to additional nature-based therapies during a rehabilitation ward period.

NCT ID: NCT05854056 Not yet recruiting - Rehabilitation Clinical Trials

Tibial Tubercle Distalisation and Accelerated Rehabilitation

Start date: September 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare in distalising tibial tubercle osteotomy procedure group fast rehabilitation to traditional rehabilitation. The main questions it aims to answer are: - Will the novel accelerated rehabilitation protocol lead to faster recovery and improved functional outcome at 6, 12 and 24 weeks compared with the conservative rehabilitation protocol? - Will the complication rate be similar in both groups? Participants will be following fast rehabilitation or the traditional rehabilitation guidelines after distalising tibial tubercle osteotomy procedure according to the randomisation. Researchers will compare fast rehabilitation group to the traditional rehabilitation group to see if recovery and functional outcome is improved in fast rehabilitation group and complication rate will be similar in both groups.

NCT ID: NCT05831618 Not yet recruiting - Rehabilitation Clinical Trials

New Rehabilitation Protocol for Patients With PPPD

Start date: July 30, 2023
Phase: N/A
Study type: Interventional

The investigators will test a new rehabilitation protocol on patients with persistent postural perceptual dizziness (PPPD). The investigators hypothesize that patients with PPPD, in the absence of vestibular deficits, do not benefit from standard vestibular rehabilitation but instead need a rehabilitation that acts on visual and postural stability, through training of saccadic movements in dynamic contexts of cognitive-motor dual-task and rehabilitation of postural stability.

NCT ID: NCT05821335 Not yet recruiting - Rehabilitation Clinical Trials

Leap Motion Based Gamefication Exercises in the Individuals With Systemic Sclerosis

Start date: May 30, 2023
Phase: N/A
Study type: Interventional

Leap Motion Based Gamefication Exercises in the Individuals With Systemic Sclerosis

NCT ID: NCT05177380 Not yet recruiting - Rehabilitation Clinical Trials

Efficacy of a Personalized Rehabilitation Program of Facial Involvement in Systemic Sclerosis

PREVISS
Start date: September 2022
Phase: N/A
Study type: Interventional

Systemic sclerosis is a rare autoimmune disorder characterized by microangiopathy, activation of the immune system, and sclerosis of tissues including the skin. Facial involvement is frequent and disabling. It causes significant functional and aesthetic discomfort, and a major deterioration in quality of life. It results in a loss of suppleness of the skin and subcutaneous tissues, dysfunction of the temporomandibular joint, peribuccal rhagades, microstomia, and dry mouth causing difficulties in mouth opening, feeding, dental care, and weight loss. Facial involvement in systemic sclerosis can be assessed using the Mouth Handicap in Systemic Sclerosis (MHISS) score, a validated patient questionnaire assessing the functional and aesthetic consequences of systemic sclerosis on the face. Although common and disabling, facial involvement is underestimated and poorly managed. Immunosuppressive and/or anti-fibrosis drugs are not very effective. Facial rehabilitation could significantly improve the mouth handicap but facial rehabilitation is not currently performed in standard care in systemic sclerosis patients. The aim of the study is to evaluate the efficacy of a personalized rehabilitation program vs standard care in facial involvement of systemic sclerosis patients.