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Pre-pain rehabilitation (PREPARE) treatment in chronic pain: a randomized controlled trial (RCT)

1. What is the effectiveness of MIP (MI-based pre-treatment) compared to UC (usual care) on the level of participation and treatment drop-out in patients with chronic non-specific musculoskeletal pain following pain rehabilitation?2. What is the…

Vitamin D and non-specific musculoskeletal complaints in non-Western immigrants

We aim to assess the effect of high-dose vitamin D supplementation on non-specific musculoskeletal complaints in non-Western vitamin D-deficient immigrants and to determine whether improvement of mood is associated with this effect.

The (cost-)effectiveness of PREPARE (Pre-pain rehabilitation) treatment, a Motivational interviewing (MI)-based nurse-led intervention on motivation and adherence for, and participation after pain rehabilitation treatment in chronic non-specific musculoskeletal pain syndrome patients: a randomized controlled trial (RCT).

The primary objective of this current project is to study the (cost-) effectiveness of Motivational interviewing in non-specific musculoskeletal chronic pain patients who are indicated for pain rehabilitation treatment. It is hypothesized that an MI…

A multicentre, single blinded, randomized controlled trial on the (cost) effectiveness of a prevention course on reducing or preventing disabilities from musculoskeletal complaints in music students at Dutch conservatories.

Primary Objective:Is a prevention program, based on principles of health behavior change, education about playing-related musculoskeletal disorders and postural training, more effective in preventing and/ or reducing disabilities from…

*Pain exposure* physical therapy versus standard therapy for patients with complex regional pain syndrome type 1 (CRPS-1)

Despite a lacking scientific argumentation, the PEPT approach or Macedonian therapy, is now being adopted on a large scale among physical therapists in The Netherlands for patients with CRPS-1. There are two level C retrospective cohort studies…

Study on the effect of pain medication on functional capacity and self reported disability in patients with chronic low back pain;
a triple blinded RCT

This study aims to investigate the effect of analgetics on a functional capacity evaluation (FCE) and self reported disability in patients with CLBP.

A comparison between intensive lumbar extensor resistance training and usual care provided by the GP for chronic a-specific low back pain patients: a RCT

To compare the effects of intensive resistance training of the lumbal extensors with usual care as provided and prescribed by the GP, for patients with chronic a-specific low back pain.

Effectiveness of a multidisciplinary team care programme in comparison with usual care for patients with sclerodermia: a randomised, controlled trial.

Research question: Is a group-based, multidisciplinary treatment programme more effective than usual care in patients with systemic sclerosis?

A Randomized, Double-Blind, Placebo- and Active-Controlled Study of
DS-5565 in Subjects with Pain Associated with Fibromyalgia.

The primary objective is to compare change in weekly average daily pain score (ADPS) from baseline to Week 13 in subjects receiving either dose of DS-5565 versus placebo. Weekly ADPS is based on daily pain scores reported by the subject that best…

The effects of additional protein intake on muscle strength and physical performance in physically active elderly

Therefore the present study is designed to investigate the impact of additional protein intake on muscle strength and physical performance in physically active elderly. Moreover, muscle mass will be determined. Furthermore, we assess the influence…

Active Vibration Induced Treatment by Abdominal Excitation

1. To investigate the tolerability and safety of HALF-MIS used in elderly patients with chronic musculoskeletal pain.2. To investigate the effect on pain of HALF-MIS used in elderly patients with chronic musculoskeletal pain.3. To investigate the…

A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of IgPro20 (Subcutaneous Immunoglobulin, Hizentra®) in Adults with Dermatomyositis (DM) - The RECLAIIM Study

The primary objective of this study is to assess the efficacy of IgPro20 0.5 g/kg weekly subcutaneous (SC) doses in comparison to placebo in adult subjects with DM, as measured by responder status based on the Total Improvement Score (TIS)…