- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT02475005
An Intervention to Improve Adolescent Headache Self-management (TH)
Studieöversikt
Status
Intervention / Behandling
Detaljerad beskrivning
Headaches dramatically affect adolescents' overall functioning and quality of life. We have developed a highly engaging mobile-based program that will help adolescents to make connections between behaviors and symptoms, and to ultimately improve functioning and quality of life. The mobile-based program will provide a state of the art pain tracker, a variety of coping strategies, and information about self-management of symptoms. This app will offer a maximally engaging way to help adolescents track their pain, make connections between lifestyle and pain, and learn key self-management skills.
The study involves the participant being randomized into either the experimental group, where he/she will be using this mobile application to track their headache symptoms, or the control group, where he/she will receive headache treatment as usual; the control group will not be using an app for this study. The intervention will last for two months.
Participants will be assessed at baseline, at 2-months post baseline, at 3-months post baseline, and at 6-months post baseline. All participants will be asked to complete online questionnaires about their headaches. We plan to enroll 144 adolescent participants with headaches, as well as one caregiver (meaning a parent/guardian) for each adolescent.
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
Massachusetts
-
Newton, Massachusetts, Förenta staterna, 02464
- Inflexxion
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
[The above age limits are specific to adolescent participants.]
Inclusion Criteria - Adolescents
- Between ages 13 and 17 (inclusive)
- Able to read and speak English
- Has recurring headaches that are not related to another medical condition
- iPhone user with access to an iPhone [4/4S or later] for use during the intervention period
Exclusion Criteria - Adolescents
- Secondary headache or seizure disorder. Examples include: increased intracranial pressure, hydrocephalus, traumatic brain injury, benign or cancerous brain
- Cognitive impairment or psychiatric condition that would interfere with ability to use the mobile application or complete the assessments
Inclusion Criteria - Caregivers
Parent or guardian of an adolescent who meets the above eligibility criteria for adolescent participants
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Experimentell: Mobile self management app on smartphone
|
|
Inget ingripande: Treatment as usual
Treatment as usual (control group)
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Change in pain coping at 2 months, 3 months, and 6 months post-baseline
Tidsram: 2 months, 3 months, 6 months
|
Measured by Pain Coping Questionnaire (PCQ) - Reid et al., 1998
|
2 months, 3 months, 6 months
|
Change in headache intensity at 2 months, 3 months, and 6 months post-baseline
Tidsram: 2 months, 3 months, 6 months
|
"In the past 7 days, how would you rate your headache pain on average..." from 0-no pain to 10-worst possible pain
|
2 months, 3 months, 6 months
|
Change in headache frequency at 2 months, 3 months, and 6 months post-baseline
Tidsram: 2 months, 3 months, 6 months
|
On how many days during the past 30 days have you had a headache?
How many days in the past 30 were you completely headache free?"
|
2 months, 3 months, 6 months
|
Change in quality of life at 2 months, 3 months, and 6 months post-baseline
Tidsram: 2 months, 3 months, 6 months
|
Measured by PedMIDAS - Hershey et al., 2001
|
2 months, 3 months, 6 months
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Change in pain self-efficacy at 2 months, 3 months, and 6 months post-baseline
Tidsram: 2 months, 3 months, 6 months
|
Measured by Pain Self-Efficacy Scale - Burch, Tsao, et al., 2006
|
2 months, 3 months, 6 months
|
Change in school absenteeism at 2 months, 3 months, and 6 months post-baseline
Tidsram: 2 months, 3 months, 6 months
|
Ask caregivers: "How many full school days did your child miss in the past 30 days due to headaches?"
|
2 months, 3 months, 6 months
|
Change in physical and psychosocial functioning at at 2 months, 3 months, and 6 months post-baseline
Tidsram: 2 months, 3 months, 6 months
|
Measured by parent report version of the PedsQL 4.0 (Varni et al., 1999)
|
2 months, 3 months, 6 months
|
Change in health care utilization at 2 months, 3 months, and 6 months post-baseline
Tidsram: 2 months, 3 months, 6 months
|
Measured by asking caregiver to report information such as the following:
|
2 months, 3 months, 6 months
|
Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 2R44HD066920-03A1 (U.S.S. NIH-anslag/kontrakt)
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