Positive PsychoTherapy in Acquired Brain Injury (ABI) Rehabilitation (PoPsTAR)

NHS Trust

Status: Completed

Conditions: Emotional Distress; Acquired Brain Injury

Treatments: Other: Psychotherapy

Study type: Interventional

Funder types: Other

Identifiers

NCT01867684

GN12CP391

CZH/4/778 (Other Grant/Funding Number)

Details and patient eligibility

About

Stroke, head injury and other forms of brain injury are a major cause of physical, psychological and social disability in the adult population. Psychological distress is common following brain injury, but the evidence base for specific psychotherapeutic methods in this population is limited, and standard treatment approaches may not be suitable. Recently there has been a growing interest in positive psychology - the study of wellbeing, positive emotions and characteristics, and personal growth. The investigators believe that positive psychotherapy interventions may be beneficial after acquired brain injury, to reduce psychological morbidity. Because such interventions have not previously been applied in this population, the investigators propose to conduct a pilot randomised controlled trial to examine the feasibility of a brief positive psychotherapy intervention in an out-patient setting. This project will produce essential information to allow us to plan future full-scale clinical trials in this area.

Enrollment: 37 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Aged 18 years or over;
• Diagnosis of stroke or acquired brain injury (confirmed clinically and/or radiologically);
• Between 3 and 12 months post-injury at time of recruitment;
• Presence of emotional distress (score in moderate or above range on at least one sub-scale of the Depression Anxiety Stress Scales; DASS-21);
• Medically stable;
• Able to consent to research.

Exclusion criteria

• Significant communication impairments that would preclude participation;
• Diagnosis of mild traumatic brain injury (due to the known additional complexities contributing to outcome in this population);
• Comorbid developmental learning disability or degenerative neurological condition.

Pre-injury history of mood disorder will not lead to exclusion.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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37 participants in 2 patient groups

Treatment as usual

No Intervention group

Description:

Standard NHS care for the patient group (NHS care will vary as participants will be recruited from a variety of NHS clinics).

Psychotherapy

Experimental group

Description:

Brief psychotherapy intervention delivered over 8 weeks in addition to standard care.

Treatment:

Other: Psychotherapy