Recruiting NCT05677412
Sleep, Pain and Stress in Adolescents With Persistent Pain
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 →
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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