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Recruiting NCT05677412

Sleep, Pain and Stress in Adolescents With Persistent Pain

No phase Interventional Pain, Chronic Sleep

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: suggestive relaxation, Neutral story.
Who it may be relevant to
Registry conditions: Pain, Chronic, Sleep. Basic parameters: 15 years — 17 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Finland
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The main aim is the gain information of sleep structures in adolescents with persistent pain. Also to study simple interventions to support their sleep and pain management. The main aim of this study is to test the efficacy and feasibility of suggestive presleep relaxation technique in improving sleep quality and sleep-related emotional memory processing.

Interventions

  • Behavioral suggestive relaxation
    suggestive story before sleep onset
  • Behavioral Neutral story
    neutral story before sleep

Primary outcome measures

  • Sleep quality [Time frame: one night]

Eligibility criteria

Inclusion criteria

  • Patients aged 15-17 years with persistent (> 3months) pain reporting average pain intensity over 3/10 on the Numerical Rating Scale (NRS).

Exclusion criteria

  • ongoing medication for sleep or pain.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Crossover
Masking
Open label
Primary purpose
Treatment

Study locations

Finland · 1 center
  • New Childrens Hospital — Helsinki

Identifiers

NCT: NCT05677412 · ULSHelsinki

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗