Skip to content

Stress Management Intervention in Inner City Adolescents With Asthma

Pilot Study: Stress Management Intervention as a Tool for Managing Persistent Asthma in Inner City Adolescent Patients.

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01445015
Acronym
SIPIICAA
Enrollment
50
Registered
2011-10-03
Start date
2011-07-31
Completion date
2012-06-30
Last updated
2011-10-03

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

Conditions

Asthma, Psychosocial Stress

Keywords

adolescents

Brief summary

The study will utilize a stress management program delivered over 10 sessions that is hypothesized to result in decreased stress levels and improved coping strategies in an inner city adolescent asthma population. Participants will include adolescents ages 10-15 years with physician diagnosed asthma. The outcome measures will be obtained via psychosocial questionnaires and spirometry.

Interventions

10 session intervention utilizing a cognitive behavorial program with a goal of stress reduction

OTHERPeer viewed movies

PG rated movies to be viewed over 10 sessions in peer setting

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
8 Years to 15 Years
Healthy volunteers
Yes

Inclusion criteria

* Ages 8-15 years of age * Physician diagnosed asthma based on NHBLI guidelines * English speaking * Child assent/parental consent

Exclusion criteria

* Refusal of child assent/parental consent * Non-English speaking * History of psychiatric illness, autoimmune disease, HIV/AIDs, smoking history.

Design outcomes

Primary

MeasureTime frame
Scope of change in perceived stress from enrollment to completion of study using the Perceived stress scale5 weeks

Secondary

MeasureTime frame
Secondary outcomes within scope of change from enrollment to completion of study in coping as assessed by Kidcope5 weeks
Secondary outcomes within scope of change from enrollment to completion of study in anxiety as measured by State Trait Inventory5 weeks
Secondary outcomes within scope of change from enrollment to completion of study in quality of life as assessed by PAQLQ5 weeks

Countries

United States

Contacts

Primary ContactLisa Moreno, MD
lim2022@med.cornell.edu718-350-6680

Outcome results

None listed

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