The Newcastle COPD CBT CARE Study

Conditions

Anxiety, depression, respiratory. Mental and Behavioural Disorders Anxiety, depression, respiratory.

L S, V W, R S, Mj K, H P, Sjc T.

2022-06-063 citations

The TANDEM trial: protocol for the process evaluation of a randomised trial of a complex intervention for anxiety and/or depression in people living with chronic obstructive pulmonary disease (COPD).

Kelly M, Steed L, Sohanpal R, Pinnock H, Barradell A, Dibao-Dina C, Mammoliti KM, Wileman V, Rowland V, Newton S, Moore A, Taylor S.

2021-07-269 citations

10.1186/s13063-021-05460-w

Tailored, psychological intervention for anxiety or depression in people with chronic obstructive pulmonary disease (COPD), TANDEM (Tailored intervention for ANxiety and DEpression Management in COPD): protocol for a randomised controlled trial.

Sohanpal R, Pinnock H, Steed L, Heslop Marshall K, Chan C, Kelly M, Priebe S, Roberts CM, Singh S, Smuk M, Saqi-Waseem S, Healey A, Underwood M, White P, Warburton C, Taylor SJC, TANDEM Investigators.

2020-01-0625 citations

10.1186/s13063-019-3800-y

Efficacy of a minimal home-based psychoeducative intervention versus usual care for managing anxiety and dyspnoea in patients with severe chronic obstructive pulmonary disease: a randomised controlled trial protocol

Dorthe Gaby Bové, Dorthe Overgaard, Kirsten Lomborg, Bjarne Ørskov Lindhardt, Julie Midtgaard

BMJ Open2015-07-0126 citations

10.1136/bmjopen-2015-008031

Effectiveness of cognitive behavioural therapy (CBT) interventions for anxiety in patients with chronic obstructive pulmonary disease (COPD) undertaken by respiratory nurses: the COPD CBT CARE study: (ISRCTN55206395).

Heslop K, Newton J, Baker C, Burns G, Carrick-Sen D, De Soyza A.

2013-11-0422 citations

10.1186/1471-2466-13-62

Interventions

As of 14/10/2016: The two interventions were: 1. Group A – CBT Arm (Brief CBT treatment delivered by respiratory nurses). Group A received a brief CBT

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patient with a confirmed diagnosis of COPD (FVC/FEV1 ratio 50% predicted) and severe to very severe (8 4. Willing to participate in the study and able to provide written informed consent 5. Agreed to attend a minimum of 2 and maximum of 6 CBT sessions 6. Target Gender: Male & Female 7. Lower Age Limit 18 years

Exclusion criteria

Exclusion criteria: 1. Patients with HADSA score <8 (within normal range) 2. Patients with known psychosis and personality disorders 3. Patients currently receiving psychological therapy including counselling, psychotherapy including CB 4. Patients unable to engage in CBT e.g. cognitive impairment or dementia) 5. Patients with limited verbal and/or written communication problems

Design outcomes

Primary

Measure	Time frame
Does CBT delivered by respiratory nurses reduce anxiety (1.5 points on HADS scale).; Timepoint(s): At 3 months	—

Secondary

Measure	Time frame
1. Does CBT delivered by respiratory nurses reduced anxiety & depression compared to standard care measured at timepoint(s) 6 & 12 months 2. Reduction in Hospital Anxiety & Depression Scale of at least 1.5 points compared to standard care measured at timepoint(s): 6 months & 12 months	—

Countries

United Kingdom

Outcome results

None listed