University of the Fraser Valley — Biomedical Watch V2

Traitements2programmes

Essais1liés

Publications0liées

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Traitements

2

Molécule	Indication / population	Phase	Objectif	Pays	Résultat
Evaluation of a Mind-body Based Application for the Treatment of Chronic/Persistent Pain.We are investigating the effects of a mind-body based mobile application on the experience of chronic pain. Participants meeting our criteria for chronic pain (confirmed via self-report) will complete an online baseline questionnaire. Eligible participants will be enrolled in the study and randomized into control (usual care, waitlisted) or intervention group (6-week mind-body based mobile application intervention). Randomization will be stratified by pain intensity and gender using computer-generated block randomization to create varying block sizes of 4 and 8. We will run the trial in multiple cohorts in series to obtain desired sample size. All participants will complete online questionnaires at baseline and post-intervention at 6 weeks that measure pain intensity, interference with daily living, pain perceptions, mental health outcomes, and medication use. Participants will also complete weekly questionnaires on weeks 2 to 6 to gauge frequency of application usage (intervention) or other pain treatments (control). Participants in the intervention group will be asked to repeat the follow-up questionnaire at 12-weeks.	Migraine	NA	Traitement symptomatique	Canada	À vérifier
Evaluation of a Mind-body Based Application for the Treatment of Chronic/Persistent Pain.We are investigating the effects of a mind-body based mobile application on the experience of chronic pain. Participants meeting our criteria for chronic pain (confirmed via self-report) will complete an online baseline questionnaire. Eligible participants will be enrolled in the study and randomized into control (usual care, waitlisted) or intervention group (6-week mind-body based mobile application intervention). Randomization will be stratified by pain intensity and gender using computer-generated block randomization to create varying block sizes of 4 and 8. We will run the trial in multiple cohorts in series to obtain desired sample size. All participants will complete online questionnaires at baseline and post-intervention at 6 weeks that measure pain intensity, interference with daily living, pain perceptions, mental health outcomes, and medication use. Participants will also complete weekly questionnaires on weeks 2 to 6 to gauge frequency of application usage (intervention) or other pain treatments (control). Participants in the intervention group will be asked to repeat the follow-up questionnaire at 12-weeks.	Migraine	NA	Traitement symptomatique	Canada	À vérifier

Essais cliniques

1

Molécule	Indication / population	Phase	NCT	Titre	Statut
Evaluation of a Mind-body Based Application for the Treatment of Chronic/Persistent Pain.	Migraine	NA	NCT05090683	Evaluation of a Mind-body Based Application for the Treatment of Chronic/Persistent Pain.	COMPLETED

Publications

0

Molécule	Indication / population	Titre	Journal	Date
Aucune publication.