Randomisation Sample Clauses

Randomisation. The randomisation will be done in a 2:2:1:1 ratio to one of four treatment sequences: Sequence Subjects Treatment 1 Subsequent retreatment(s) 1 110 subjects 600 U Dysport® 600 U Dysport® 2 110 subjects 800 U Dysport® 800 U Dysport® 3 55 subjects Placebo 600 U Dysport® 4 55 subjects Placebo 800 U Dysport® During analysis of study Treatment 1, the two placebo containing sequences will be pooled into a single arm. Randomisation will be stratified by:
Sample 1Sample 2
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Randomisation. Eligible and consenting participants were randomised to the CTI or TAU by block randomisation, stratified by prison, after participants had been consented and baseline assessments were complete. Participants were fully informed about the randomisation procedure and knew that they may receive CTI or TAU. Randomisation was undertaken by the King's Clinical Trials Unit, utilising a process of concealment, using an online system and there was full allocation concealment. Data were entered onto the online InferMed MACRO data entry system that is managed by the King’s Clinical Trials Unit. The researcher was notified of the randomisation outcome immediately and communicated this information to the participant, the CTI manager and to the clinical team. Because of the nature of the intervention, it was not possible to blind participants, researchers, CTI managers or mental health inreach team staff to the treatment allocation. The researchers were required to review participants’ prison and community mental health records, where information on allocation was usually present, and the project’s funding did not allow arrangements to avoid this. In addition, the researchers were based in the mental health inreach team office along with the CTI manager and information regarding allocation was displayed in this office.
Sample 1
Randomisation. Randomisation was made using 40 closed envelopes each containing a piece of paper with either Mindfulness or Relaxation written on it. After participants completed the measures, the researcher picked one envelope and allocated the participant to the assigned intervention.
Sample 1

Related to Randomisation

  • Immunisation 7.4.1 The parties agree in principle that responsibility for pre-exposure immunisation of employees rests with employers who should accept responsibility for safety in the workplace, advised as necessary by health officials.

  • Study An application for leave of absence for professional study must be supported by a written statement indicating what study or research is to be undertaken, or, if applicable, what subjects are to be studied and at what institutions.

  • Grievance Initiation 33. a. A grievance affecting more than one employee shall be filed with the departmental official having authority over all employees affected by the grievance.

  • Stabilisation In connection with the distribution of any Notes, any Dealer designated as a Stabilisation Manager in the applicable Final Terms may over-allot or effect transactions which support the market price of the Notes at a level higher than that which might otherwise prevail, but in doing so such Dealer shall act as principal and not as agent of the Issuer. Any stabilisation will be conducted in accordance with all applicable regulations. Any loss resulting from over-allotment and stabilisation shall be borne, and any net profit arising therefrom shall be retained, as against the Issuer, by any Stabilisation Manager for its own account.

  • Random Testing Notwithstanding any provisions of the Collective Agreement or any special agreements appended thereto, section 4.6 of the Canadian Model will not be applied by agreement. If applied to a worker dispatched by the Union, it will be applied or deemed to be applied unilaterally by the Employer. The Union retains the right to grieve the legality of any imposition of random testing in accordance with the Grievance Procedure set out in this Collective Agreement.

  • Random Drug Testing All employees covered by this Agreement shall be subject to random drug testing in accordance with Appendix D.

  • Third Party Verification 4.8.1 The SPD shall be further required to provide entry to the site of the Power Project free of all encumbrances at all times during the Term of the Agreement to SECI and a third Party nominated by any Indian Governmental Instrumentality for inspection and verification of the works being carried out by the SPD at the site of the Power Project.

  • Hospitalisation Where a Subsidised Resident is admitted to hospital for treatment or to undergo an assessment, we will continue to make payments in full for up to 21 days (or for any longer period that the NASC Service may recommend) in any one of our financial years;

  • Clinical 2.1 Provides comprehensive evidence based nursing care to patients including assessment, intervention and evaluation.

  • Protocol No action to coerce or censor or penalize any negotiation participant shall be made or implied by any other member as a result of participation in the negotiation process.

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