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Sleep, Pain and Stress in Adolescents With Persistent Pain

Sleep, Pain and Stress in Adolescents With Persistent Pain

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05677412
Acronym
PedPainSleep
Enrollment
20
Registered
2023-01-10
Start date
2023-05-23
Completion date
2026-06-30
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Chronic, Sleep

Brief summary

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

BEHAVIORALsuggestive relaxation

suggestive story before sleep onset

BEHAVIORALNeutral story

neutral story before sleep

Sponsors

University of Helsinki
CollaboratorOTHER
Helsinki University Central Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Experimental within-subject study design

Eligibility

Sex/Gender
ALL
Age
15 Years to 17 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Sleep qualityone nightThe overnight PSG (Somnomedics) is used to measure sleep during two nights (Somnomedics, Somnoscreen plus HD), with the following recorded parameters: electroencephalography (left and right for F, C, O); left and right eletrooculogram; left and right electromyogram; electrocardiogram. Sleep recordings are done with portable devices so that the patients will sleep at their home during the recordings.

Countries

Finland

Contacts

Primary ContactReetta M Sipilä, PhD
reetta.sipila@hus.fi+358406812427

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026