Chronic Obstructive Pulmonary Disease and Health Coaching

NCT ID: NCT05711654

Last Updated: 2023-02-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-01

Study Completion Date

2023-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of this study is to determine the effect of the health coaching approach applied to patients with Chronic Obstructive Pulmonary Disease on the perceived social support of the patients.

Research Hypotheses:

H0: Health coaching approach has no effect on perceived social support in patients with COPD.

H1: Health coaching approach has an effect on perceived social support in patients with COPD.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The current study is in the design of a single-blind randomized controlled trial. Patients were randomized into intervention group (n:34) and control group (n=34). Coaching interview will be held once a week for 6-8 weeks with the patients in the coaching group. Coaching sessions will be based on the social support the patient receives from family and friends.

Both the coaching group and the control group will be given information about COPD. This information will be given face to face first. Later, the booklet of the training given will be delivered to the patients via message.

The data was collected using the socio-demographic information form,COPD Assessment Test (CAT), and Multidimensional Scale of Perceived Social Support (MSPSS).

Data Analysis will be done with SPSS package program

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Chronic Obstructive Pulmonary Disease

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Factorial Assignment
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants
None (Open Label)

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Health coaching group

The patients in the health coaching group will first be given data collection tools, and then the COPD patient information training created by the researcher will be given.

For the first eight weeks after the training, face-to-face meetings will be held with patients once a week.

Data collection tools will be applied to the patients again in the fourth week and 12 weeks after the interviews are over.

Group Type EXPERIMENTAL

Health coaching

Intervention Type BEHAVIORAL

Coaching interview will be held with patients at regular intervals.

Control group

Data collection tools will be applied to the patients in the control group first, and then the COPD patient information training created by the researcher will be given.

After the training, there will be no interviews with the patients, and data collection tools will be applied again in the 12th and 20th weeks.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Health coaching

Coaching interview will be held with patients at regular intervals.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* over 40 years old,
* diagnosed with COPD for at least 6 months,
* without stage III and IV heart failure,
* without any cancer diagnosis,
* no communication problems (such as those who do not have problems in expressing - themselves, no hearing problems),
* not diagnosed with cognitive and mental dysfunction (such as Alzheimer's, dementia, bipolar disorder, major depression)
* Patients who agree to participate in the study will be formed.

Exclusion Criteria

* with any cancer
* with stage IV heart failure
* patients requiring clinical follow-up due to acute COPD exacerbation
Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Osmaniye Korkut Ata University

OTHER

Sponsor Role collaborator

Harran University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Derya TÜLÜCE

Faculty of Health Sciences

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Derya Tülüce, PhD

Role: PRINCIPAL_INVESTIGATOR

Osmaniye Korkut Ata University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Osmaniye Korkut Ata University

Osmaniye, Center, Turkey (Türkiye)

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Derya Tülüce, PhD

Role: CONTACT

+905052933587

Derya Tülüce, PhD

Role: CONTACT

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Derya TULUCE, PhD, RN

Role: primary

+905052933587

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Osmaniye Korkut Ata University

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Telerehabilitation in COPD
NCT05053061 RECRUITING NA