A Psychomotor Group Intervention for Young Adults With Anxiety Symptoms
25. juni 2026 oppdatert av: VIA University College
Development and Feasibility of a Group-based Psychomotor Intervention for Anxiety in Young Adults
The goal of this clinical trial is to learn if a psychomotor (a body-oriented therapy) group intervention can be feasibly delivered to a group of young adults (age 18-35) with anxiety symptoms within a higher educational setting.
The main questions it aims to answer are:
- Is it possible to recruit and retain participants in this intervention?
- Is the intervention acceptable and tolerable to participants?
- Do participants complete the planned sessions and assessments?
Participants will:
- Attend one weekly group session over ten consecutive weeks
- Participate in active and contemplative body-based exercises
- Complete questionnaires about their mental health and interviews about their experiences of participating
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
12
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
Region Midt
-
Aarhus, Region Midt, Danmark, 8200
- VIA University College
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
Tar imot friske frivillige
Nei
Beskrivelse
Inclusion Criteria:
- Age between 18 and 34 years
- A score of at least 2 on item 10 of the Anxiety Symptom Scale (indicating the perceived strain of the experienced anxiety symptoms) and at least 1 on one or more of items 1-3 (generalized anxiety symptoms and avoidance behavior)
- Sufficient Danish language proficiency to participate in group sessions and interviews
Exclusion Criteria:
- Physical or psychological conditions that prevents participation in group-based or bodily-activities, such as significant musculoskelatal impairment or current, untreated episodes of psychosis
- Ongoing alcohol or substance abuse
- Concurrent participation in another body-oriented intervention program
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Psychomotor intervention group
|
Ten weekly sessions of a psychomotor therapy group program.
Session duration: 2½ hours.
Group size: 12 participants.
Sessions include psychoeducational content and body-oriented exercises such as breathing exercises, relaxation exercises, body scans, or grounding exercises.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Number of participants recruited
Tidsramme: For each participant: 20 minutes during the three month enrollment period.
|
Enrollment during a three month period from June 2025 to September 2025.
Enrollment interview was approximately 20 minutes.
Participants had the option of attending a one hour information meeting.
|
For each participant: 20 minutes during the three month enrollment period.
|
|
Number of participants retained
Tidsramme: From enrollment to end of intervention at 11 weeks
|
From enrollment to end of intervention at 11 weeks
|
|
|
Attendance
Tidsramme: From beginning of intervention to end of intervention at 11 weeks
|
Number of participants attending each of the ten weekly sessions
|
From beginning of intervention to end of intervention at 11 weeks
|
|
Acceptability to participants
Tidsramme: Post intervention at 12 weeks
|
Evaluated through qualitative interviews with a duration of 45-60 minutes
|
Post intervention at 12 weeks
|
|
Fidelity of the intervention
Tidsramme: From beginning of intervention to end of intervention at 11 weeks
|
The extent to which intervention components were administered as intended.
This was registered by an observer who registered any deviations from a therapy manual.
|
From beginning of intervention to end of intervention at 11 weeks
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Changes in Beck Anxiety Inventory
Tidsramme: Baseline and post-intervention at 11 weeks
|
21 items rated on a four-point Likert scale with scores ranging rom 0 (no anxiety) to 21 (worst possible anxiety)
|
Baseline and post-intervention at 11 weeks
|
|
Changes in Perceived Stress Scale
Tidsramme: Baseline and post-intervention at 11 weeks
|
Ten items rated on a five-point Likert scale with scores ranging from 0 (no stress) - 40 (maximum stress)
|
Baseline and post-intervention at 11 weeks
|
|
Changes i WHO-Five Well-Being Index
Tidsramme: Baseline and post-intervention at 11 weeks
|
A five-item measure rated on a six-point Likert scale with scores ranging from 0 (worst possible well-being) to 100 (maximum well-being)
|
Baseline and post-intervention at 11 weeks
|
|
Changes in Multiple Assessment of Interoceptive Awareness
Tidsramme: Baseline and post-intervention at 11 weeks
|
Body awareness measured through 32 items across eight subscales rated on a six-point Likert scale, reported as mean scores on each subscale (range 0-5)
|
Baseline and post-intervention at 11 weeks
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
12. september 2025
Primær fullføring (Faktiske)
18. desember 2025
Studiet fullført (Faktiske)
18. desember 2025
Datoer for studieregistrering
Først innsendt
12. juni 2026
Først innsendt som oppfylte QC-kriteriene
25. juni 2026
Først lagt ut (Faktiske)
2. juli 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
2. juli 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
25. juni 2026
Sist bekreftet
1. juni 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 9001099
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
UBESLUTTE
IPD-planbeskrivelse
Small scale feasibility study data.
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .