Skip to main content
. 2023 Oct 24;2023(10):CD014722. doi: 10.1002/14651858.CD014722.pub2

Cerquera Córdoba 2021.

Study characteristics
Methods Study design: RCT
Duration of study: the study was conducted from February 2019 to February 2020.
Country: Colombia
Income classification: upper‐middle‐income country in 2019‐2020
Geographical scope: Bucaramanga and its metropolitan area
Healthcare setting: patient's homes (home‐care companies with nursing assistants)
Participants 1. Age: average age of caregivers 55.1 years
2. Gender: both
3. Socioeconomic background: median socioeconomic level (64%)
4. Educational background: secondary education level or less (58%)
Inclusion criteria:
a. being a relative of the patient;
b. living in the same home;
c. performing the role of caregiver for at least 8 hours a day for more than 3 months;
d. receiving no remuneration.
Exclusion criteria:
ceasing to be the main caregiver, unpaid, for reasons such as prolonged hospitalization (more than 20 days), institutionalization, or death of the patient
Note: at baseline, the total sample score for the Zarit Burden Interview (ZBI) at baseline was 45 (16.8).
Stated purpose: to evaluate the efficacy of a multicomponent programme with transdisciplinary intervention to reduce the burden and improve social support of caregivers of patients with Alzheimer's
Interventions Name: respite care group; multicomponent plus respite care group
Title/name of PW and number
Intervention 1: transdisciplinary work of 6 psychologists, 4 physiotherapists, 4 speech therapists
Intervention 2: nursing assistants (for respite group)
1. Selection: home care provider company
2. Educational background: not specified
3. Training: for respite group nursing assistants trained in the proper handling of patients and support in the execution of activities of daily living—8 hours transdisciplinary team (6 psychologists, 4 physiotherapists, 4 speech therapists)
4. Supervision: not specified
5. Incentives/remuneration: not specified
Prevention type: selective prevention – participants were included based upon the presence of a risk factor (being caregivers of patients with Alzheimers) and presented distress levels at baseline well below the cut‐off for the measure.
Intervention details
Respite care group: relay “breathing”. Respite care was carried out for 8 weeks, once a week with a duration of 4 hours per day, by nursing assistants through a home care provider company.
Multicomponent plus respite care group: multicomponent, integrated by the components of psychoeducation, systemic communication, and physiotherapy, with the objectives of favouring the management of body posture, movements, and physical activity, as well as promoting assertive communication where the quality of communication and affectivity was recognized, through the transdisciplinary work of 6 psychologists, 4 physiotherapists, and 4 speech therapists, who had academic sufficiency in the subject. The multicomponent intervention was carried out for 8 weeks. This intervention group also received the “relay breathing” intervention.
Control: waiting list – no intervention (delivery of respite intervention at the end of the study)
Outcomes Participants’outcomes of interest for this review
  1. Distress/PTSD symptoms – ZBI

  2. Social outcomes (social support) – Social Support Medical Outcomes Study Questionnaire (MOS)


Note: we included data from the respite care group intervention and control.
Carers’outcomes of interest for this review
Nil
Economic outcomes
Nil
Time points: baseline, post‐intervention (< 1 month post‐intervention; 7‐24 months post‐intervention)
Notes Source of funding: Ministry of Science, Technology and Innovation (MINCIENCIAS)
Notes on validation of instruments (screening and outcomes): for the ZBI, the version by Martín‐Carrasco and colleagues was used. This tool presents good reliability and validity for the Colombian population. The MOS has a reliability evaluation for Colombia (Cronbach's alpha between 0.921 to 0.736).
Additional information: none
Handling the data: not applicable
Prospective trial registration number: not specified