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Effectiveness of a Cognitive-behavioral Program of Coping With Psychological Stress in People With Retinitis Pigmentosa (RCT)

U

University of Granada (UGR)

Status

Completed

Conditions

Self Efficacy
Psychopathy
Vision Disorders
Stress, Psychological

Treatments

Behavioral: A cognitive-behavioral intervention program
Other: Standard intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT03368027
Retinitis pigmentosa RCT

Details and patient eligibility

About

The aim of this study is to evaluate the efficacy of cognitive - behavioral therapy for the control of psychopathological stress and the disease of people with Retinitis Pigmentosa (RP).

Full description

This randomized controlled trial aims to evaluate the efficacy of cognitive - behavioral therapy for the control of psychopathological stress and the disease of people with Retinitis Pigmentosa (RP) on aspects such as vulnerability to stress, perceived stress, psychopathological state, general self-efficacy, resilience, satisfaction with social support and visual field. This study has two groups: 1) cognitive - behavioral therapy group, and 2) Standard intervention or control group. The two interventions will be conducted for 3 months (with a total of 12 sessions), one session per week, with a duration of 90 minutes per session.

Enrollment

30 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosed with Retinitis Pigmentosa (legally blind RP patients).
  • meet the membership criteria of the Spanish National Association of ONCE.
  • having a reduction of the visual field of at least 10 degrees in both eyes
  • having an age between 18 and 65 years.

Exclusion criteria

  • no visual remainders (advanced retinosis).
  • no studies.
  • cognitive impairment, determined by the Spanish Mini-Mental State Examination - MMSE test.
  • mobility problems
  • high risk of falls associated with retinosis, measured by the Morse scale, with a score over 50 points.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

Stress management program
Experimental group
Description:
A cognitive-behavioral program of coping with psychological stress for 3 months (with a total of 12 sessions), one session per week, with a duration of 90 minutes per session.
Treatment:
Behavioral: A cognitive-behavioral intervention program
Standard intervention
Active Comparator group
Description:
Usual activities performed in the association where they attend (supervised by a psychologist) for 3 months (with a total of 12 sessions), one session per week, with a duration of 90 minutes per session.
Treatment:
Other: Standard intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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