Clinical trials

5

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

Condition / disease
Location
Status: Recruiting

Positive Feeding of the Preterm Infant

The goal of this feasibility study is to assess the feasibility to implement a feeding strategy for preterm infants. The main questions it aims to answer are: * Is it feasible to implement the PoP-intervention in a level 3a category Neonatal intensive care unit? * Is the PoP-intervention acceptable for parents of preterm infants and health care personnel working in Neonatal intensive care unit? Parents of preterm infants and health care personnel will be asked to follow a protocol of a feeding strategy based on the preterm infants development and cues throughout the NICU-stay.

Participants needed: 15
Trial details
Biological sex: AllType: InterventionalSponsor: Oslo Metropolitan UniversityUpdated: Aug 11, 2025Locations: 1
Eligibility criteria

gestational age of 28 weeks [+1]

diagnoses or malformations that makes eating difficult [+3]

Status: Recruiting

The Mother in Norway Study

The Norwegian government is implementing the Nurse Family Partnership program (NFP) to combat child abuse and social inequality. This study will examine NFP with an individually randomized controlled parallel-group trial. The study will enroll 700 mothers over three years, with half receiving NFP services and the other half receiving standard care. The primary outcome is violence towards mothers and their children, assessed through questionnaires and observation tests. The study will also evaluate the program's effects on various health-related outcomes using administrative data. Cost-effectiveness analyses will be conducted to compare NFP to existing services and improve its delivery efficiency.

Participants needed: 700
Trial details
Age: 16+Biological sex: FemaleType: InterventionalSponsor: Oslo Metropolitan UniversityUpdated: Aug 11, 2025Locations: 5
Eligibility criteria

Not listed

Status: Recruiting

Treatment of Phantom Limb Pain by Intensive Visual Simulation Therapy

Phantom limb pain (PLP) is reported by as much as 80 % of patients following an amputation. There is increasing knowledge of the relation between PLP and maladaptive changes in brain cortical regions. Research has shown that the sight of an "intact arm" moving in a mirror may reverse maladaptions (Mirror-therapy, MT) and reduce PLP. The current project will implement a digital and modernized version of MT, i.e. Intensive Visual Simulation Therapy (IVS-T). Pilot studies have shown promising results on pain reduction in people with phantom limb pain when using IVS-T. However, there is a lack of RCT studies on this patient population. This study is a 2-arm randomized controlled trial (RCT) investigating the effectiveness of IVS-T compared with usual care in person with unilateral upper- or lower limb amputation with chronic phantom limb pain. The primary aim of the study is to investigate if IVS treatment is superior to usual care in reducing phantom limb pain intensity after 2 months of treatment in unilateral amputees with moderate to severe PLP. The study will furthermore explore quality of life, analgesic consumption, phantom pain characteristics, mobility, and disability. In addition, the study utilizes brain imagery during treatments to investigate neural plasticity and the association between PLP and maladaptive cortical changes.

Participants needed: 38
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Oslo Metropolitan UniversityUpdated: Mar 21, 2025Locations: 1
Eligibility criteria

Unilateral or bilateral lower limb/upper limb amputees [+7]

Significant visual impairment / blind [+1]

Status: Recruiting

Support Groups - a Model for Social Inclusion and Reduction of Bullying in School

Study Title: Support Groups - a model for social inclusion and reduction of bullying in school Study Design: Cluster Randomized Controlled trial (CRCT) Objective: To investigate the effectiveness of a support group intervention using a solution-focused approach among school children in 5th-7th grade in southeastern Norway Intervention: Peer support groups with a solution-focused approach Study Population: School Children

Participants needed: 1,586
Trial details
Age: 10-12Biological sex: AllType: InterventionalSponsor: Oslo Metropolitan UniversityUpdated: Aug 29, 2024Locations: 1
Eligibility criteria

Primary Schools with more than 200 students [+1]

Primary Schools with less than 200 students

Status: Not yet recruiting

COMPRESSED - A Longitudinal Study of Compressed Work Schedules Within the Health, Care and Welfare Services

The aim of COMPRESSED is to investigate the potential consequences of a compressed work schedule within the municipal health, care and welfare services.

Participants needed: 700,000
Trial details
Biological sex: AllType: ObservationalSponsor: Oslo Metropolitan UniversityUpdated: Mar 24, 2023
Eligibility criteria

Employed within the municipal health, care and welfare services.