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Cognitive Behavioral Therapy Intervention on Mental Wellbeing among Elderly Population

Cognitive Behavioral Therapy (CBT) Intervention on Mental Wellbeing among Elderly Population: A Multi-Method Study Design

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12623001220651
Acronym
CBT Trial
Enrollment
136
Registered
2023-11-27
Start date
2024-02-26
Completion date
2024-03-25
Last updated
2023-12-04

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

Conditions

None listed

Brief summary

This trial is intended to evaluate the effectiveness of cognitive behavior therapy intervention on mental well-being (quality of life, depression, and resilience) among older adults. The study claims that older adults who will participate in CBT intervention will have effect on their mental well-being as compared to those who will not receive this intervention. The newly diagnosed older adults with depression aged between 60-74 years regardless the gender will be recruited as study participants. The data will be collected from the two largest public and private tertiary care teaching hospitals of Karachi after the approval of concerned research committees and study setting permission. The structured and validated tools geriatric depression scale and quality of life instruments will be utilized to measure the mental well-being and effectiveness of intervention among older adults. The data will be entered and analyzed statistical package of social science version.26. The results will be analyzed through both descriptive and inferential statistics.

Interventions

Cognitive Behavioral Therapy (CBT) intervention based on the Roy Adaptation Model’s concepts such as physiological, self-concept, interdependence, and role functions will be provided to evaluate the effectiveness on mental well-being (depression, quality of life, and resilience) among older adults. The model has considered is a grand nursing theory that explains the relationship between mental problems with well-being based on theoretical perspectives (Butts & Rich, 2021). The intervention aims

Cognitive Behavioral Therapy (CBT) intervention based on the Roy Adaptation Model’s concepts such as physiological, self-concept, interdependence, and role functions will be provided to evaluate the effectiveness on mental well-being (depression, quality of life, and resilience) among older adults. The model has considered is a grand nursing theory that explains the relationship between mental problems with well-being based on theoretical perspectives (Butts & Rich, 2021). The intervention aims to measure the effect on mental well-being such as thought processes, behavior, emotions, physical symptoms, functional capabilities, and socialization. Moreover, the content that will be included in the intervention is handling life situations, emotional regulations, hopefulness, managing symptoms, self-control, problem-solving strategies, and promoting positive and constructive thoughts and behaviors. This trial aims to compare the study outcome (mental well-being) through CBT intervention between the intervention and control groups. The intervention group will receive six weeks of CBT along with the treatment as usual. However, controlled group will receive treatment as usual only. The primary investigator with the collaboration of a psychologist will provide the intervention. The primary investigator is a Ph.D. Scholar and experienced mental health nurse with plenty of clinical and teaching experience of more than 12 years. The PI has experience in conducting various mental health seminars and sessions for both the general public and vulnerable populations. Moreover, psychologists will add information, plan, and guide the intervention for accurate and efficient delivery of content to the population. Six weeks of CBT intervention of six sessions will be provided to evaluate the effects on the mental well-being of older adults. For the intervention, there will be one session per week of 90 minutes, allowing the study participants to come together on one platform. The session will be taken face to face in a group of 6-8 people in the seminar room of the study setting. Attendance will be marked in each session who are receiving the intervention. In addition, for adherence to the intervention, telephonic conversation will be performed regularly with the participants and attendance checklist will be provided and monitoring will be performed by primary investigator himself.

Sponsors

Santosh Kumar
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used) (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
60 Years to 74 Years
Healthy volunteers
No

Inclusion criteria

- Early older adults - Newly diagnosed cases of depression less than or equal to one year. - Ability to speak and read Urdu / English language - Willing to participate in the study and giving consent to participate in the study

Exclusion criteria

- Individuals with hypomanic/manic episodes, cognitive impairment, or active homicidal/suicidal ideation - Individuals with severe alcoholism or substance abuse disorder - Being involved in any other intervention - Individuals with communication deficits make understanding and discussion impossible

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026