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Journaling and its impact on the quality of life of adolescents and young adults receiving palliative care

Effect of journaling on person-centric outcomes in adolescents and young adults receiving specialist palliative care: a randomized controlled trial - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094852
Enrollment
82
Registered
2025-09-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: C00-D49- Neoplasms

Interventions

Intervention1: Journaling: Total Duration: 1 month. The intervention involves guided journaling in which participants use a structured template with prompts to write about their feelings and unspoken

Sponsors

Christian Medical College Vellore
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Diagnosis of advanced cancer, i.e., any solid or hematological malignancy unlikely to be cured or controlled with treatment. - AYAs who are physically able and have the cognition to be able to think, reflect and write. - Able to read and write in a language they are familiar with.

Exclusion criteria

Exclusion criteria: 1. Cognitive impairment, confusion, or delirium prohibiting reliable self-report. 2. Sensorimotor deficits preventing participation. 3. Severe comorbid psychiatric illness.

Design outcomes

Primary

MeasureTime frame
Compare the change in patient s quality of life from baseline to day 7 between intervention arm and control arm as measured on the Functional Assessment of Chronic Therapy - Spiritual Well-being (FACIT-Sp)Timepoint: At Baseline (T0) & At 1 week (T1)

Secondary

MeasureTime frame
Compare the change in patient s quality of life from baseline to one month between intervention arm and control arm as measured on the Functional Assessment of Chronic Therapy - Spiritual Well-being (FACIT-Sp).Timepoint: T0-Day 0, T2-At one month;Compare the change in patients psychological distress from baseline to day 7 between intervention arm and control arm as measured on Hospital Anxiety and Depression Scale-Anxiety and Depression {HADS (A & D)} scores.Timepoint: T0-Day 0, T1-Day 7;Compare the change in patients psychological distress from baseline to one month between intervention arm and control arm as measured on Hospital Anxiety and Depression Scale-Anxiety and Depression {HADS (A & D)} scores.Timepoint: T0-Day 0, T2-At One Month

Countries

India

Contacts

Public ContactAby John Thampi

Christian Medical College Vellore

jenifer.jeba@cmcvellore.ac.in9360647948

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026