ArticleBMJ open2026
PRIME pilot trial: a protocol for a multicentre pilot randomised controlled trial of PRehabilitation In advance of Major Elective surgery (PRIME).
Article in BMJ open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07590141 (PRehabilitation In Advance of Major Elective Surgery), which is not on this map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
PRehabilitation In Advance of Major Elective Surgery: A Pilot Randomized Controlled Trial (PRIME Pilot)
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
introductionPrehabilitation is a promising preoperative intervention to improve patient recovery after surgery. Virtually delivered, home-based programmes represent the most efficient model for prehabilitation delivery. However, virtually delivered prehabilitation interventions remain understudied. This manuscript describes the protocol for a pilot randomised controlled trial (RCT) of a virtually monitored, home-based prehabilitation intervention. METHODS AND ANALYSIS: We will conduct a pilot RCT comparing the standard of care to a virtually monitored home-based prehabilitation programme in adults undergoing major elective intrathoracic, intra-abdominal or orthopaedic surgery. Outcome assessors will be blinded to treatment allocation. The intervention consists of 3-4 weeks of a multimodal (exercise, nutrition and psychosocial support) prehabilitation programme supported through a mobile application already in use at the Kingston Health Sciences Centre. The primary feasibility outcomes and their targets are: (1) monthly recruitment rate of >20 participants across all centres and (2) mean intervention adherence of >80%. A sample of 120 participants will be adequate to estimate recruitment and adherence rates with acceptable precision. The secondary outcomes include comparisons of complications, mortality, new-onset disability, length of stay, readmission, quality of life, nutritional status and functional capacity between intervention arms. Secondary outcomes will be collected prior to randomisation, 2 days before surgery and 30 days after surgery. ETHICS AND DISSEMINATION: Ethical approval has been granted by Clinical Trials Ontario (Project ID: 5495). Results will be disseminated through presentations at scientific conferences, peer-reviewed publications and engagement with traditional and social media. TRIAL REGISTRATION NUMBER: ClinicalTrials.gov (NCT07590141).
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