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Effectiveness of Multisensoral Nature-based Intervention in Hospitalized Children During Venous Blood Sampling

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 1 year 6 months later Dec 31, 2026 → Jun 30, 2028
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Record History

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  1. Primary and study completion pushed from Dec 31, 2026 to Jun 30, 2028 Show 9 more changesShow less
    • Recruitment opened
    • Enrollment increased: 53 → 106 participants
    • Start date: Aug 1, 2025 to Dec 1, 2026
    • Primary endpoints: details revised at 1 of 1 entry
    • Eligibility criteria expanded, about 9 words
    • Secondary endpoints: 5 to 6
    • Study description expanded, about 9 words
    • Study site revised
    • Publications: details revised at 6 of 7 entries
  2. Primary completion date: Dec 31, 2024 to Dec 31, 2026v3 Show 5 more changesShow less
    • Start date: Sep 1, 2023 to Aug 1, 2025
    • Primary endpoints: 2 to 1
    • Study completion date: May 31, 2025 to Dec 31, 2026
    • Secondary endpoints: 10 to 5
    • Study description shortened, about 4 words
  3. Re-verified, no change to tracked fieldsv2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
University of Oulu
22 trials monitored
See 2 trials at risk
Anxiety
3,263 trials monitored
See 159 trials at risk
This randomized controlled trial (RCT) study aims to evaluate the effectiveness of multisensoral nature-based intervention compare to standard care in relieving anxiety, fear and pain in hospitalized child aged 5 to 9 years and parent's anxiety and satisfaction during venous blood sampling. The assessment uses different measures to assess child's anxiety, fear, pain and parent's anxiety and satisfaction during venous blood sampling. The study also measures the time spent on blood sampling.
Trial Details
NCT Number NCT05494684
Lead Sponsor University of Oulu
Conditions
(from sponsor)		 Anxiety, Fear, Pain, Satifaction
Related terms Anxiety Disorders, Pain
Enrollment 106 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov