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Health Literacy in People With Chronic Obstructive Pulmonary Disease

Health Literacy. An Intervention on Organized Information and Health Care for People With Chronic Obstructive Pulmonary Disease (COPD)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03216603
Enrollment
130
Registered
2017-07-13
Start date
2017-11-01
Completion date
2020-12-31
Last updated
2021-12-14

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

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

Health literacy

Brief summary

Health literacy refers to personal and relational factors affecting a person's ability to acquire, understand and use information about health and health services. In a need assessment study it was found that, the health services need to focus on health literacy factors in the follow up of patients with chronic obstructive pulmonary disease (COPD). Thus, this project evaluate the effect a of a health literacy partnership health promotion intervention (hospital, municipalities, university) after discharge from hospital with the use of motivational interviewing and tailored follow-ups on re-admission, health literacy, self-management quality of life and cost in people with COPD compared with usual care.

Interventions

BEHAVIORALHealth literacy intervention group

In the health literacy intervention group all patients will receive self-management help using a motivating interviewing (MI) technique delivered by two MI and COPD trained nurses once a week for eight weeks after hospitalization. Subsequently, the contact between the patients and the nurses will be by follow up motivational telephone calls once a month or more if needed for four months (i.a a total of six months intervention period).

Sponsors

University of Oslo
CollaboratorOTHER
Norwegian Extra Foundation for Health and Rehabilitation
CollaboratorOTHER
Lovisenberg Diakonale Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed with COPD, * Above 18 years, * Admitted to a medical department at the main intervention hospital, l * Live in the sites belonging to the intervention hospital.

Exclusion criteria

* Not diagnosed with COPD, * Not above 18 years, * Not admitted to a medical department at the main intervention hospital, and * Not living in the sites belonging to the intervention hospital. * Cognitive failure * Patients that are investigated or treated for cancer

Design outcomes

Primary

MeasureTime frameDescription
Change of admissionsEight weeks, six months and one yearNumber of re-admissions

Secondary

MeasureTime frameDescription
Change of disease specific quality of lifeEight weeks, six months and one yearQuestionnaire
Change of e-HealthEight weeks, six months and one yearQuestionnaire
Change of physical functionEight weeks, six months and one yearQuestionnaire
Change of health literacyEight weeks, six months and one yearQuestionnaire
Change of psychological stressEight weeks, six months and one yearQuestionnaire
Change of self-efficacyEight weeks, six months and one yearQuestionnaire
Change of self-managementEight weeks, six months and one yearQuestionnaire

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026