A self-management programme of activity coping and education - SPACE FOR COPD - in primary care: a pragmatic trial

A self-management programme of activity coping and education - SPACE FOR COPD - in primary care: a prospective, pragmatic, single-centre, single-blinded randomised controlled trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN17942821

Enrollment

193

Registered

2015-02-11

Start date

2015-01-01

Completion date

Unknown

Last updated

2023-03-20

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

Conditions

Chronic obstructive pulmonary disease (COPD), self management Respiratory Chronic obstructive pulmonary disease, unspecified

Interventions

Those randomised to the SPACE group will be given the SPACE manual and will receive six group sessions in the community delivered by trained healthcare professionals going through various topics relat

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Established diagnosis of COPD

Exclusion criteria

Exclusion criteria: 1. Unable to participate in exercises component of rehabilitation, e.g. neurological, locomotive or psychiatric disability 2. Unable to read English to the level of an 8 year old 3. Unwilling to take part 4. Has received or participated in the Pulmonary Rehabilitation or received the SPACE manual within the last 12 months

Design outcomes

Primary

Measure	Time frame
COPD Assessment Test (CAT) at baseline, 6 months and 9 months	—

Secondary

Measure	Time frame
1. The Chronic Respiratory Questionnaire ? Self Report (CRQ-SR) at baseline, 6, 9 months for both groups 2. The Patient Activation Measure (PAM) at baseline, 6, 9 months for both groups 3. The Hospital Anxiety and Depression Scale (HADS) at baseline, 6, 9 months for both groups 4. The Bristol COPD Knowledge Questionnaire (BCKQ) at baseline, 6, 9 months for both groups 5. Exercise performance (The Incremental Shuttle Walk Test and Endurance Shuttle Walking Test) at baseline, 6, 9 months for the interventional group, at 9 months only for the usual care group 6. The EQ-5D throughout the study 7. Healthcare utilisation throughout the study 8. Smoking status throughout the study 9. Physical activity via the SenseWear Armband (SAB) at baseline, 6, 9 months for both groups	—

Measure

Time frame

1. The Chronic Respiratory Questionnaire ? Self Report (CRQ-SR) at baseline, 6, 9 months for both groups 2. The Patient Activation Measure (PAM) at baseline, 6, 9 months for both groups 3. The Hospital Anxiety and Depression Scale (HADS) at baseline, 6, 9 months for both groups 4. The Bristol COPD Knowledge Questionnaire (BCKQ) at baseline, 6, 9 months for both groups 5. Exercise performance (The Incremental Shuttle Walk Test and Endurance Shuttle Walking Test) at baseline, 6, 9 months for the interventional group, at 9 months only for the usual care group 6. The EQ-5D throughout the study 7. Healthcare utilisation throughout the study 8. Smoking status throughout the study 9. Physical activity via the SenseWear Armband (SAB) at baseline, 6, 9 months for both groups

—

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 26, 2026